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

BIOPSY FORCEPS

K Number: K892252 · Decision Oct 3, 1989
Classifications
1
FEI Numbers
188
Registration Numbers
188
Same Product Code
38
Applicant Total
76
Review Days
182

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Basic Information

Device Name
BIOPSY FORCEPS
K Number
K892252
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Zinnanti Surgical Instruments, Inc.
Date Received
April 4, 1989
Decision Date
October 3, 1989
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

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Other Clearances by Zinnanti Surgical Instruments, Inc.

K Number Device Name
K925501 NYLON COATED SPECULA
K941458 UTERINE MANIPULATOR/INJECTOR WITH SPRING
K941457 UTERINE INJECTOR WITH SPRING
K925560 ZSI LOOP, ZSI BALL & ZSI NEEDLE ELECTRODES
K925957 SCISSORS FOR LAPAROSCOPIC SURGERY OB/GYN USE
K925960 FORCEPS FOR LAPAROSCOPIC SURGERY OB/GYN USE
K926021 NEEDLE HOLDERS & ACCESS FOR LAPAR SURG-OB/GYN USE
K925958 SCISSOR FOR LAPAROSCOPIC SURGERY GU USE
K926181 ZSI LAPAROSCOPES-GENERAL & PLASTIC SURGERY
K926016 NEEDLE HOLDERS & ACCESS FOR LAPAR SURG-GU USE
Search all 76 clearances from Zinnanti Surgical Instruments, Inc. →