MODIFIED LUXAR LX-20 FAMILY CO2 LASER SYSTEM


Device Classification Name

powered laser surgical instrument

510(k) Number K960475
Device Name MODIFIED LUXAR LX-20 FAMILY CO2 LASER SYSTEM
Applicant
LUXAR CORP.
columbia square
555 thirteenth st., n.w.
washington, d.c., 
DC 
20004 -1109

Applicant Contact jonathan s kahn
Correspondent
LUXAR CORP.
columbia square
555 thirteenth st., n.w.
washington, d.c., 
DC 
20004 -1109

Correspodent Contact jonathan s kahn
Regulation Number 878.4810
Classification Product Code
GEX  
Date Received 02/01/1996
Decision Date 04/26/1996
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