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

HEARTPORT ENDOAORTIC CLAMP CATHETER

K Number: K974175 · Decision Dec 16, 1997
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
22
Applicant Total
24
Review Days
40

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Basic Information

Device Name
HEARTPORT ENDOAORTIC CLAMP CATHETER
K Number
K974175
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4075
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Heartport, Inc.
Date Received
November 6, 1997
Decision Date
December 16, 1997
Product Code
DWZ
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
DWZ Device, Biopsy, Endomyocardial

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DWZ), 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
K972570 HEARTPORT INTRODUCER SHEATH
K971291 HEARTPORT ENDOARTERIAL RETURN CANNULA
K970496 HEARTPORT MAZE SYSTEM: CRYOPROBE SET
K964302 HEARTPORT THORACIC TROCAR
K964161 HEARTPORT ENDOAORTIC CLAMP
Search all 24 clearances from Heartport, Inc. →