Kapp Surgical Instrument, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Michler-Kapp Cardiovascular Vent Catheter, KAPP BARI-RING ENDOSCOPIC MARKER, MODEL K-9536, KAPP BARI-RING, MODEL KS-BR-2005
9
Total
9
Cleared
0
Denied
FDA 510(k) Regulatory Record - Kapp Surgical Instrument, Inc. Cardiovascular ✕
1 devices