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source DB |
source ID
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text
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size
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updated at |
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# proj.
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# Ann.
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updated_at |
| DevicePMAs@therightstef |
P880086_S204 |
Approval for the new sustain xl pacemaker models, predicated off the victory/zephyr family of pacemaker. the device, as modified, will be marketed under the trade name sustain xl dr/sr and sustain xl |
1.49 KB |
2020-03-03 |
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9 |
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41 |
-
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| DevicePMAs@therightstef |
P910023_S061 |
Approval for a downsized version of the photon udr/vr device. The device, as modified, will be marketed under the trade name st. jude medical epic vr/dr implantable cardioverter defibrillators (model |
380 Bytes |
2020-03-03 |
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10 |
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0 |
-
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| DevicePMAs@therightstef |
P920015_S022 |
Approval for model 6726 df-1 y-adaptor/extender kit. The device is indicated to adapt two df-1 lead connectors to a single df-1 compatible connector port and/or will extend the length of a df-1 lead |
291 Bytes |
2020-03-03 |
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11 |
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0 |
-
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| DevicePMAs@therightstef |
P910023_S066 |
Approval for the identity adx models xl dr 5386 and dr 5380 pulse generators and programmer software model 3307 v4.2a. These devices are indicated as follows: implantation of identity adx models5386 |
1.18 KB |
2020-03-03 |
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11 |
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0 |
-
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| DevicePMAs@therightstef |
P980023_S019 |
Approval for modifications to the kentrox family of implantable cardioverter defibrillator (icd) leads. The devices, as modified, will be marketed under the trade names kentrox rv, kentrox rv steroid |
356 Bytes |
2020-03-03 |
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11 |
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0 |
-
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| DevicePMAs@therightstef |
P910077_S037 |
Approval for the ventak prizm 2 vr/dr models 1860/1861, ventak prizm vr/dr models 1850/1851/1855/1856, ventak prizm vr/dr he models 1852/1853, ventak mini iv models 1790/1793/1796 and ventak mini iii |
598 Bytes |
2020-03-03 |
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11 |
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0 |
-
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| DevicePMAs@therightstef |
P980016_S492 |
Approval for the mycarelink smart monitor used with the device. The device, as modified, will be marketed under the trade name mycarelink smart monitor andthe mycarelink heart application and is indi |
639 Bytes |
2020-03-03 |
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11 |
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0 |
-
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| DevicePMAs@therightstef |
P980023_S025 |
Approval for the lumax implantable cardioverter defibrillators (icds), models 300 vr, 340 vr, 300 vr-t, 340 vr-t, 300 dr, 340 dr, 300 dr-t, 340 dr-t, 300 hf, 340 hf, 300 hf-t and 340 hf-t and programm |
628 Bytes |
2020-03-03 |
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11 |
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0 |
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| DevicePMAs@therightstef |
P950022_S017 |
Approval for the addition of a fluoroscopic marker in the helix tip and the addition of new lead lengths and minor modifications to the suture sleeve. The leads are indicated for permanent sensing an |
297 Bytes |
2020-03-03 |
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11 |
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0 |
-
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| DevicePMAs@therightstef |
P980050_S000 |
Approval for the medtronic(r) jewel(r) af 7250 dual chamber implantable cardioverter defibrillator (icd), model 9961 programmer application software, and medtronic(r) sprint(tm) model 6943 steroid elu |
500 Bytes |
2020-03-03 |
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11 |
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0 |
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