C02 LASER MULTIPULSE


information about

Device Classification Name

powered laser surgical instrument

510(k) Number K002032
Device Name C02 LASER MULTIPULSE
Original Applicant
ASCLEPION-MEDITEC AG
2525 mc gaw ave.
irvine, 
CA 
92623 -9791

Original Contact william kelley
Regulation Number 878.4810
Classification Product Code
GEX  
Date Received 07/03/2000
Decision Date 09/11/2000
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

Type Traditional
Reviewed by Third Party No

Combination Product

No