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

WILTEK GRASPING FORCEPS

K Number: K894862 · Decision Dec 21, 1989
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
73
Applicant Total
21
Review Days
143

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Basic Information

Device Name
WILTEK GRASPING FORCEPS
K Number
K894862
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Wiltek Medical, Inc.
Date Received
July 31, 1989
Decision Date
December 21, 1989
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

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Other Clearances by Wiltek Medical, Inc.

K Number Device Name
K990231 WILTEK HOT BIOPSY FORCEPS
K922989 WILTEK IRRIGAITON/ASPIRATION TUBE SET
K930419 WILTEK BIOPSY FORCEPS
K914882 WILTEK BALLOON CHOLANGIOGRAPHY CATHETER
K914881 WILTEK LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER
K914132 WILTEK ELECTROCAUTERY ACTIVE CORD
K914131 WILTEK ELECTROCAUTERY ADAPTOR
K912122 CHOLANGIOGRAPHY CATHETER
K912288 WILTEK STANDARD CHOLANGIOGRAPHY CATHETER
K910334 ELECTROCAUTERY PROBE
Search all 21 clearances from Wiltek Medical, Inc. →