ENDOSCOPIC LASER DELIVERY SYSTEM-LASERTX


Device Classification Name

powered laser surgical instrument

510(k) Number K023257
Device Name ENDOSCOPIC LASER DELIVERY SYSTEM-LASERTX
Original Applicant
PROSURG, INC.
2193 trade zone blvd.
san jose, 
CA 
95131

Original Contact ashvin desai
Regulation Number 878.4810
Classification Product Code
GEX  
Date Received 09/30/2002
Decision Date 03/28/2003
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

statement

statement

Type Traditional
Reviewed by Third Party No

Combination Product

No