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

NUVOLASE 532 CUTANEOUS LASER SYSTEM

K Number: K990780 · Decision Mar 22, 1999
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
5
Review Days
13

Basic Information

Device Name
NUVOLASE 532 CUTANEOUS LASER SYSTEM
K Number
K990780
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4810
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
AMERICAN LASER MEDICAL
Date Received
March 9, 1999
Decision Date
March 22, 1999
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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