FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

HIRSCH BIPOLAR COAGULATION FORCEPS AND ADAPTOR CABLES

K Number: K942319 · Decision Jun 8, 1994
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
16
Review Days
26

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Basic Information

Device Name
HIRSCH BIPOLAR COAGULATION FORCEPS AND ADAPTOR CABLES
K Number
K942319
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Berchtold Holding GmbH
Date Received
May 13, 1994
Decision Date
June 8, 1994
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

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Other Clearances by Berchtold Holding GmbH

K Number Device Name
K083066 CHROMOPHARE E 778 AND E 558
K080857 CHROMOPHARE E-SERIES
K024132 CHROMOPHARE X 65
K990656 CHROMOPHARE D 530 LDR SURGICAL LIGHT
K991527 CHROMOPHARE D500, D530, D650
K974433 CHROMOPHARE D 500, CHROMOPHARE D 530
K965130 CHROMOPHARE
K955750 TELETOM
K950932 BIPOLAP HOOK ELECTRODE
K944855 CHROMOPHARE
Search all 16 clearances from Berchtold Holding GmbH →