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

BIPOLAR BIOPSY FORCEPS

K Number: K904985 · Decision Jan 25, 1991
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
45
Applicant Total
21
Review Days
84

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Basic Information

Device Name
BIPOLAR BIOPSY FORCEPS
K Number
K904985
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4300
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Everest Medical Corp.
Date Received
November 2, 1990
Decision Date
January 25, 1991
Product Code
KGE
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KGE Forceps, Biopsy, Electric

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Other Clearances by Everest Medical Corp.

K Number Device Name
K003060 PLASMAKINETIC GENERATOR
K000496 EVERSHEARS BIPOLAR SCISSORS
K993412 BITX PROBES
K994336 BITX PROBES
K971565 BICOAG COAGULATING FORCEPS
K955001 EVERSHEARS SCISSORS, BILAP PROBES, BICOAG FORCEPS
K945975 EVERSHEARS(R) SCISSORS, BILAP(R) PROBES, BICOAG(R) FORCEPS
K922509 LAPAROSCOPIC ELECTROSURG DEVICE W/IRRIGA & ASPIRA
K922246 TUBING SET W/ IRRIGATION & ASPIRATION VALVING
K920089 MONOPOLAR COAGULATING POLYPECTOMY SNARE
Search all 21 clearances from Everest Medical Corp. →