age_PMA_annotations

Documents (2,258) JSON TSV

source DB	source ID	text	size	updated at	# proj.	updated_at
DevicePMAs@therightstef	P990071_S004	Approval for the addition of a stockert remote control and connection cable. The device, as modified, will be marketed under the trade name stockert remote control and connection cable and is indicat	357 Bytes	2020-03-03	13	-
DevicePMAs@therightstef	P970007_S000	Approval for the IMx(R) Tacrolimus II Assay. This device is indicated for use as an in-vitro reagent sytemf or the quantitative determination of tacrolimus and some metabolites in human whole blood a	284 Bytes	2020-03-03	13	-
DevicePMAs@therightstef	P160003_S000	Approval for the PRO-Kinetic Energy Cobalt Chromium (CoCr) Coronary Stent System. This device is indicated for improving coronary luminal diameter in patients with de novo or restenotic lesions in nat	313 Bytes	2020-03-03	11	-
DevicePMAs@therightstef	P020047_S004	Approval for the 2.75 mm line extension for the multi-link vision coronary stent system. The device is indicated for improving coronary luminal diameter in patients with abrupt or threatened abrupt c	359 Bytes	2020-03-03	11	-
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	-
DevicePMAs@therightstef	P980001_S000	approval for the NIR ON(TM) Ranger(TM) and NIR ON(TM) Ranger(TM) w/SOX(TM) Premounted Stent Systems. The device is indicated for improving coronary luminal diamter in the following patient subsets:	716 Bytes	2020-03-03	11	-
DevicePMAs@therightstef	P990040_S000	Approval for the trufill(r) n-butyl cyanoacrylate (n-bca) liquid embolic system. The device is indicated for the embolization of cerebral arteriovenous malformations (avms) when presurgical devascula	220 Bytes	2020-03-03	13	-
DevicePMAs@therightstef	P890023_S011	Approval for the hydrogenics 60 (ocufilcon f) uv in-monomer tint contact lens indicated for extended wear (up to 7 days / 6 nights between removals for cleaning and disinfection). The device, as modi	1.62 KB	2020-03-03	11	-
DevicePMAs@therightstef	P110032_S010	Approval for a line extension that would include two larger size stent grafts. the device, as modified, will be marketed under the trade name aorfix and aorfix plus aaa flexible stent graft system wit	825 Bytes	2020-03-03	11	-
DevicePMAs@therightstef	P880086_S088	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	11	-