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

FUJINON FORCEPS -- MODIFICATION

K Number: K922396 · Decision Dec 10, 1992
Classifications
1
FEI Numbers
188
Registration Numbers
188
Same Product Code
38
Applicant Total
21
Review Days
205

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Basic Information

Device Name
FUJINON FORCEPS -- MODIFICATION
K Number
K922396
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Hobbs Medical, Inc.
Date Received
May 19, 1992
Decision Date
December 10, 1992
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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