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
FDA 510(k) Regulatory Record - Appriva Medical, Inc. Cardiovascular ✕
2 devices