MILESMAN PREMIUM


Device Classification Name

powered laser surgical instrument

510(k) Number K073300
Device Name MILESMAN PREMIUM
Applicant
MILESMAN S.L.
55 northern blvd.
suite 200
great neck, 
NY 
11021

Applicant Contact natalya valerio
Regulation Number 878.4810
Classification Product Code
GEX  
Date Received 11/23/2007
Decision Date 12/04/2007
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