Heartport, Inc.
Heartport, Inc. holds FDA 510(k) medical device clearances, first cleared 1996, most recent 2000.
Top product codes for Heartport, Inc.
Recent clearances by Heartport, Inc.
- K994243 — DIRECTFLOW KIT, 24 FR, SOFTCLAMP KIT, 24FR, STRAIGHTSHOT KIT, 23 FR, STRAIGHT TIP, STRAIGHTSHOT KIT, 23 FR, ANGLED TIP
- K981995 — QUICKDRAW VENOUS CANNULA
- K990772 — DIRECTFLOW ARTERIAL CANNULA
- K981009 — HEARTPORT ENDOPULMONARY VENT CATHETER
- K974736 — HEARTPORT DIRECT AORTIC RETURN CANNULA WITH INTRODUCER
- K974175 — HEARTPORT ENDOAORTIC CLAMP CATHETER
- K972570 — HEARTPORT INTRODUCER SHEATH
- K971291 — HEARTPORT ENDOARTERIAL RETURN CANNULA
- K964302 — HEARTPORT THORACIC TROCAR
- K970496 — HEARTPORT MAZE SYSTEM: CRYOPROBE SET
- K964161 — HEARTPORT ENDOAORTIC CLAMP
- K965051 — HEARTPORT NEEDLE TROCAR
- K962835 — HEARTPORT ENDOVENOUS DRAINAGE CANNULA
- K964248 — HEARTPORT ENDOCORONARY SINUS CATHETR
- K961333 — HEARTPORT MULTIFIRE CLIP APPLIER
- K961334 — HEARTPORT HANDSWITCH ELECTROCAUTERY PROBE
- K962366 — HEARTPORT CABLE BULLDOG CLAMP
- K961463 — HEARTPORT THORACIC SURGICAL TROCARS: (TOST-4-3, TOSTL-6-3, TON-4-2 AND TONL-6-2
- K962858 — HEARTPORT ENDOVASCULAR CARDIOPULMONARY BYPASS SYSTEM ANTEGRADE SYTEM (CATALOG NUMBER ECPB-A) ANTEGRADE/RETROGRADE SYSTEM
- K962510 — HEARTPORT ENDOAORTIC CLAMP
- K961245 — HEARTPORT ENDOPULMONARY VENT
- K961270 — HEARTPORT ENDOSINUS CATHETER
- K955132 — HEARTPORT ENDOAORTIC CLAMP
- K955121 — HEARTPORT ENDOARTERIAL RETURN CANNUAL
Data sourced from openFDA. This site is unofficial and independent of the FDA.