VIVASCOPE SYSTEM, MODEL 1500, 3000


Device Classification Name

light, surgical, floor standing

510(k) Number K080788
Device Name VIVASCOPE SYSTEM, MODEL 1500, 3000
Applicant
LUCID, INC.
2320 brighton henrietta
townline rd
rochester, 
NY 
14623

Applicant Contact james joy
Correspondent
LUCID, INC.
2320 brighton henrietta
townline rd
rochester, 
NY 
14623

Correspodent Contact james joy
Regulation Number 878.4580
Classification Product Code
FSS  
Date Received 03/20/2008
Decision Date 09/17/2008
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