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

A.C.L. GUIDE KIT

K Number: K862564 · Decision Aug 18, 1986
Classifications
1
FEI Numbers
526
Registration Numbers
526
Same Product Code
18
Applicant Total
55
Review Days
46

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Basic Information

Device Name
A.C.L. GUIDE KIT
K Number
K862564
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Aspen Laboratories, Inc.
Date Received
July 3, 1986
Decision Date
August 18, 1986
Product Code
FZX
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
FZX Guide, Surgical, Instrument

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