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

M.R. ASSOC. TRIPOD GRASPING FORCEPS

K Number: K800972 · Decision May 8, 1980
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
72
Applicant Total
15
Review Days
15

Basic Information

Device Name
M.R. ASSOC. TRIPOD GRASPING FORCEPS
K Number
K800972
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
MR ASSOCIATES, INC.
Date Received
April 23, 1980
Decision Date
May 8, 1980
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

Similar 510(k) Clearances

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Other Clearances by MR ASSOCIATES, INC.

K Number Device Name
K800970 M.R. ASSOC. BASKET RETRIEVERS
K800962 M.R. ASSOC. WASHING TUBE/MEASURING TUBE
K800971 M.R. ASSOC. MAGNETIC EXTRACTOR
K800976 M.R. ASSOC. W TYPE GRASPING FORCEPS
K800966 M.R. ASSOC. CYTOLOGY BRUSHES
K800975 M.R. ASSOC. TRUE-FEEL HANDLE
K800969 M.R. ASSOC. CANNULAS
K800965 M.R. ASSOC. SNARES; CRESCENT SNARE WIRE
K800963 BIOPSY FORCEPS W/NEEDLE M.R. ASSOC.
K800967 M.R. ASSOC. ALLIGATOR GRASPONG FORCEPS
Search all 15 clearances from MR ASSOCIATES, INC. →