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

BIOSPSY FORCEPS

K Number: K920762 · Decision Aug 26, 1992
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
73
Applicant Total
34
Review Days
189

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Basic Information

Device Name
BIOSPSY FORCEPS
K Number
K920762
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Symbiosis Corp.
Date Received
February 19, 1992
Decision Date
August 26, 1992
Product Code
OCZ
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
OCZ Endoscopic Grasping/Cutting Instrument, Non-Powered

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (OCZ), ordered by most recent decision date.

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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
K932266 SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN
Search all 34 clearances from Symbiosis Corp. →