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

HEARTPORT THORACIC TROCAR

K Number: K964302 · Decision May 9, 1997
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
50
Applicant Total
24
Review Days
192

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Basic Information

Device Name
HEARTPORT THORACIC TROCAR
K Number
K964302
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1390
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Heartport, Inc.
Date Received
October 29, 1996
Decision Date
May 9, 1997
Product Code
DRC
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
DRC Trocar

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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
K964161 HEARTPORT ENDOAORTIC CLAMP
Search all 24 clearances from Heartport, Inc. →