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

GIP/MEDI-GLOBE BIOPSY FORCEPS

K Number: K941359 · Decision Jul 12, 1994
Classifications
1
FEI Numbers
195
Registration Numbers
195
Same Product Code
38
Applicant Total
18
Review Days
113

Basic Information

Device Name
GIP/MEDI-GLOBE BIOPSY FORCEPS
K Number
K941359
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MEDI-GLOBE CORP.
Date Received
March 21, 1994
Decision Date
July 12, 1994
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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