age_PMA_annotations

Documents (2,258) JSON TSV

source DB	source ID	text	size	updated at	# proj.	updated_at
DevicePMAs@therightstef	P830026_S074	Approval for Rx7000 Programming System Model 522-17 with R1.00.00 Software. The device, as modified, will be marketed under the trade name Rx7000 Model 522-17 Porgrammer and is indicated for the inte	265 Bytes	2020-03-03	11	-
DevicePMAs@therightstef	P010015_S368	Approval for an update to the indications for use to include pacing at the bundle of His. The device, as modified, will be marketed under the trade name SelectSecure MRI SureScan Lead Model 3830 and i	459 Bytes	2020-03-03	9	-
DevicePMAs@therightstef	P010015_S005	Approval for the insync iii model 8042 and insync iii model 9981 application software which is indicated as follows: the insync iii model 8042 device is indicated for the reduction of symptoms of mod	742 Bytes	2020-03-03	11	-
DevicePMAs@therightstef	P960040_S235	Approval for incepta, energen. punctua and teligen icd models and the incepta, energen. punctua and cognis crt-d models and prm software application model 2868 and pulse generator software. the device	854 Bytes	2020-03-03	11	-
DevicePMAs@therightstef	P010012_S031	Approval for the addition of wandless telemetry to your currently market-approved crt-d devices that will allow communication with the programmer at an increased distance. the device, as modified, wil	552 Bytes	2020-03-03	11	-
DevicePMAs@therightstef	N970003_S000	Approval for your product development protocol (pdp) for the: guidant pulsar models 470, 970, 972, 1172, 1272 pulse generators, guidant pulsar max models 1170, 1171, 1270 pulse generators, and guidant	1.43 KB	2020-03-03	11	-
DevicePMAs@therightstef	P010015_S006	Approval for the medtronic/vitatron carelink programmer model 2090, model 2067 carelink programmer rf head, model 2290 lead analyzer, model 2292 analyzer cable, model 2091 carelink programmer modem, m	1.56 KB	2020-03-03	11	-
DevicePMAs@therightstef	P010012_S160	Approval for the acuity spiral lead model 4591, 4592, and 4593. The device is indicated for chronic, left-ventricular pacing and sensing via the coronary veins when used in conjunction with a compati	220 Bytes	2020-03-03	10	-
DevicePMAs@therightstef	P010012_S230	Approval for a modification to the indications for use for the cognis crt-d models n118, n119; liviancrt-d models h220, h225, h227 and h229; and contak renewal 3 rf he crt-d modelsh210, h215, h217, h	812 Bytes	2020-03-03	11	-
DevicePMAs@therightstef	P960040_S029	Approval for the addition of atrial arrhythmia therapies to the vitality aicd system. The device, as modified, will be marketed under the trade name vitality avt and programmer software application m	786 Bytes	2020-03-03	11	-