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

HEARTPORT HANDSWITCH ELECTROCAUTERY PROBE

K Number: K961334 · Decision Nov 15, 1996
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
24
Review Days
221

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Basic Information

Device Name
HEARTPORT HANDSWITCH ELECTROCAUTERY PROBE
K Number
K961334
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Heartport, Inc.
Date Received
April 8, 1996
Decision Date
November 15, 1996
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GEI), 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. →