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

REPROCESSED LASER PROBE

K Number: K012682 · Decision Nov 8, 2001
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
59
Review Days
86

Basic Information

Device Name
REPROCESSED LASER PROBE
K Number
K012682
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
STERILMED, INC.
Date Received
August 14, 2001
Decision Date
November 8, 2001
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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