PMA_age_indications

Documents (2,236) JSON TSV

source DB	source ID	text	size	updated at	# proj.	updated_at
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_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	-
DevicePMAs@therightstef	P960040_S035	Approval for a fast-charge version of the device (model a155) and to correct software anomalies (models a155 and a135). The device, as modified, will be marketed under the trade name ventak vitality	768 Bytes	2020-03-03	11	-
DevicePMAs@therightstef	P950037_S042	Approval for modifications to the selox sr pacing lead family to change the steroid dosage, maximum lead body diameter, and ring electrode base material, as well as other minor changes. The device, a	365 Bytes	2020-03-03	11	-
DevicePMAs@therightstef	P830045_S109	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	-
DevicePMAs@therightstef	P880086_S146	Approval for the zephyr xl sr model 5626 pacemaker which utilizes the xl battery model 9438 which is currently approved for use with the marketed zephyr xl dr 5826 pacemaker. The device, as modified,	320 Bytes	2020-03-03	11	-
DevicePMAs@therightstef	P880086_S139	Approval for the zephyr pulse generators models: xl dr 5826, dr 5820 and sr 5620. The device is indicated in the following permanent conditions, when associated with symptoms including, but not limit	1.27 KB	2020-03-03	11	-