LASERSYSTEM BEAUTYSTAR 532


Device Classification Name

powered laser surgical instrument

510(k) Number K021975
Device Name LASERSYSTEM BEAUTYSTAR 532
Original Applicant
ASCLEPION-MEDITEC AG
8884 warner ave.
suite 167
fountian valley, 
CA 
92708

Original Contact william kelly
Regulation Number 878.4810
Classification Product Code
GEX  
Date Received 06/17/2002
Decision Date 09/13/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No