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

I.C. MEDICAL ADJUSTABLE DIRECT COUPLER

K Number: K900511 · Decision May 1, 1990
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
14
Review Days
88

Basic Information

Device Name
I.C. MEDICAL ADJUSTABLE DIRECT COUPLER
K Number
K900511
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
I.C. MEDICAL, INC.
Date Received
February 2, 1990
Decision Date
May 1, 1990
Product Code
GEX
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
GEX Powered Laser Surgical Instrument

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