Q-PLUS T


Device Classification Name

powered laser surgical instrument

510(k) Number K073549
Device Name Q-PLUS T
Applicant
QUANTA SYSTEM, S.P.A.
via iv novembre,116
solbiate olona(va), 

IT

21058

Applicant Contact isabella carrer
Regulation Number 878.4810
Classification Product Code
GEX  
Date Received 12/18/2007
Decision Date 02/28/2008
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

summary

summary

Type Traditional
Reviewed by Third Party Yes

Combination Product

No

Recalls CDRH Recalls