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

HEWSON A.C.L. GUIDE SET

K Number: K872608 · Decision Sep 16, 1987
Classifications
1
FEI Numbers
87
Registration Numbers
87
Same Product Code
19
Applicant Total
83
Review Days
72

Basic Information

Device Name
HEWSON A.C.L. GUIDE SET
K Number
K872608
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4930
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
CONCEPT, INC.
Date Received
July 6, 1987
Decision Date
September 16, 1987
Product Code
KGS
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KGS Retention Device, Suture

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