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

LASERTX - DIODE LASER & DELIVERY SYSTEM

K Number: K060326 · Decision Apr 5, 2006
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
14
Review Days
55

Basic Information

Device Name
LASERTX - DIODE LASER & DELIVERY SYSTEM
K Number
K060326
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
PROSURG, INC.
Date Received
February 9, 2006
Decision Date
April 5, 2006
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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