Appriva Medical, Inc. is one of 16567 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Appriva Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MODIFICATION TO: X-SEPT TRANSSEPTAL SHEALTH AND TRANSITION CATHETER (WITH DILATOR), MODELS PL-12-12-09, PL-12-12-10, X-SEPT TRANSSEPTAL SHEATH AND TRANSITION CATHETER, MODEL MV-03-09-90, MV-03-10-90, MV-03-11-90, MV-03-09-120, MV-03-10-1
2
Total
2
Cleared
0
Denied
Appriva Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 2 cleared submissions from 2001 to 2001. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Appriva Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Appriva Medical, Inc.
2 devices