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

LASER SYSTEM YELLOWSTAR

K Number: K013940 · Decision Feb 26, 2002
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
5
Review Days
89

Basic Information

Device Name
LASER SYSTEM YELLOWSTAR
K Number
K013940
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
ASCLEPION-MEDITEC AG
Date Received
November 29, 2001
Decision Date
February 26, 2002
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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