DIOLASE 980 D LASER SYSTEM


Device Classification Name

powered laser surgical instrument

510(k) Number K023547
Device Name DIOLASE 980 D LASER SYSTEM
Original Applicant
AMERICAN DENTAL TECHNOLOGIES, INC.
12 prairie falcon
aliso viejo, 
CA 
92656

Original Contact marcia van valen
Regulation Number 878.4810
Classification Product Code
GEX  
Date Received 10/21/2002
Decision Date 04/15/2003
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