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

SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN

K Number: K932266 · Decision Mar 15, 1994
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
45
Applicant Total
34
Review Days
329

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Basic Information

Device Name
SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN
K Number
K932266
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4300
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Symbiosis Corp.
Date Received
April 20, 1993
Decision Date
March 15, 1994
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 Symbiosis Corp.

K Number Device Name
K955119 SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES
K953453 SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES
K953242 SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODES
K952432 SYMBIOSIS BIPOLAR FORCEPS
K951387 SYMBIOSIS BIPOLAR SCISSORS
K950286 SYMBIOSIS BIPOLAR SCISSORS
K946238 SYMBIOSIS GASTROINTESTINAL BIOPSY FORCEPS
K930773 SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS
K941426 SYMBIOSIS REUSABLE MONOPOLAR ELECTROSURGICAL PROBE
K931957 SYMBIOSIS DISPOSABLE UROLOGICAL BIOPSY FORCEPS
Search all 34 clearances from Symbiosis Corp. →