LUMENIS ULTRAPULSE ENCORE CARBON DIOXIDE SURGICAL LASERS AND DELIVERY DEVICE ACCESSORIES


Device Classification Name

powered laser surgical instrument

510(k) Number K022060
Device Name LUMENIS ULTRAPULSE ENCORE CARBON DIOXIDE SURGICAL LASERS AND DELIVERY DEVICE ACCESSORIES
Original Applicant
LUMENIS, INC.
2400 condensa st.
santa clara, 
CA 
95051 -0901

Original Contact anne worden
Regulation Number 878.4810
Classification Product Code
GEX  
Date Received 06/25/2002
Decision Date 10/30/2002
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