Heartport, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DIRECTFLOW KIT, 24 FR, SOFTCLAMP KIT, 24FR, STRAIGHTSHOT KIT, 23 FR, STRAIGHT TIP, STRAIGHTSHOT KIT, 23 FR, ANGLED TIP, QUICKDRAW VENOUS CANNULA, DIRECTFLOW ARTERIAL CANNULA
24
Total
24
Cleared
0
Denied
FDA 510(k) Regulatory Record - Heartport, Inc. General & Plastic Surgery ✕
2 devices