FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

FORCEPS, BIOPSY, NON-ELECTRIC

K Number: K952863 · Decision Jul 19, 1995
Classifications
1
FEI Numbers
188
Registration Numbers
188
Same Product Code
38
Applicant Total
23
Review Days
27

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Basic Information

Device Name
FORCEPS, BIOPSY, NON-ELECTRIC
K Number
K952863
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Annex Medical, Inc.
Date Received
June 22, 1995
Decision Date
July 19, 1995
Product Code
FCL
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
FCL Forceps, Biopsy, Non-Electric

Similar 510(k) Clearances

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Other Clearances by Annex Medical, Inc.

K Number Device Name
K954377 FORCEPS, GRASPING, FLEXIBLE ENDOSCOPIC
K951532 METAL URETERAL BASKET STONE DISLODGER
K951761 METEL URETERAL BASKET STONE DISLODGER
K934636 ANNEX MEDICAL FLAT WIRE STONE EXTRACTOR
K934675 METAL URETERAL BASKET STONE DISLODGER
K934598 GRASPING FORCEPS OR RETRIEVAL FORCEPS
K925267 GRASPING FORCEPS OR RETRIEVAL FORCEPS
K925559 BILIARY STONE DISLODGER
K921401 BIOPSY FORCEPS
K924027 DISLODGER, STONE, BASKET, URETERAL, METAL
Search all 23 clearances from Annex Medical, Inc. →