FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

HEARTPORT ENDOAORTIC CLAMP

K Number: K964161 · Decision Apr 4, 1997
Classifications
1
FEI Numbers
186
Registration Numbers
186
Same Product Code
203
Applicant Total
24
Review Days
169

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Basic Information

Device Name
HEARTPORT ENDOAORTIC CLAMP
K Number
K964161
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4450
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Heartport, Inc.
Date Received
October 17, 1996
Decision Date
April 4, 1997
Product Code
DXC
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DXC Clamp, Vascular

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DXC), ordered by most recent decision date.

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Other Clearances by Heartport, Inc.

K Number Device Name
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
K970496 HEARTPORT MAZE SYSTEM: CRYOPROBE SET
K964302 HEARTPORT THORACIC TROCAR
Search all 24 clearances from Heartport, Inc. →