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> DevicePMAs@therightstef
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DevicePMAs@therightstef
P890003_S309
Approval for the viva/brava quadripolar cardiac resynchronization therapy defibrillator (crt-d) devices and is indicated for patients who require ventricular antitachycardia pacing and ventricular def
619 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P010031_S416
Approval for software changes to the mycarelink patient monitor m2.5 model 24950 with model 24955 rf head which supports the devices and medtronics reveal insertable cardiac monitors models 9529, 9528
349 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P950037_S050
Approval for modifications to the cardiomessenger and cardiomessenger ii used with the referenced devices. The devices, as modified, will be marketed under the trade names: cardiomessenger tline and
315 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P880006_S052
Approval for the model 3330 version6.1.1 software for the model 3650 merlin patient care system and model 3307 version 6.4.1 software for the model 3510 programmer which enables v-v timing, af suppres
538 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P960013_S018
Approval to modify the lead insulation on the tendril st 1788t/tc and tendril st 1782 leads, and to reduce the outer coil wire diameter on the tendril st 1782 lead. The devices, as modified, will be
655 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P890003_S252
Approval of an mr-conditional system permitting implanted patients to undergo mri scans provided specified conditions are met. The devices, as modified, make up the advisa dr mri surescan system and
1.67 KB
2020-03-03
11
0
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DevicePMAs@therightstef
P950037_S048
Approval for an additional trade name for the market approved setrox s lead, as well as minor changes to the accessories, packaging, and labeling. The device, as modified, will be marketed under the
438 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P980035_S360
Approval for software changes to the mycarelink patient monitor m2.5 model 24950 with model 24955 rf head which supports the devices and medtronics reveal insertable cardiac monitors models 9529, 9528
349 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P890003_S131
Approval for removal of the contraindication: ?patients whose primary disorder is bradyarrhythmia? and for the medtronic consulta crt-d d224trk, maximo ii crt-d d284trk medtronic secura dr d224drg, m
1.65 KB
2020-03-03
11
0
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DevicePMAs@therightstef
P950037_S078
Approval for introduction of the lumax 540 vr-t dx implantable cardioverter defibrillator (icd), a single lead icd system used in conjunction with the currently approved kainox a+ icd lead. The devic
442 Bytes
2020-03-03
11
0
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