New Depilase FDA 510(k)


#1

510(k) Number K020697
Device Name DEPILASE TWIN YAG LASER SYSTEM
Applicant
DEPILASE GROUP LTD.
ONE CANADA SQUARE
CANARY WHARF
LONDON, UK E14 5 DYContact MARIO RUSSO
Product Code GEX
Date Received 03/04/2002
Decision Date 04/12/2002
Decision SUBSTANTIALLY EQUIVALENT (SE)
Classification Advisory Committee General & Plastic Surgery
Review Advisory Committee General & Plastic Surgery
Statement/Summary/Purged Status Summary only
Type Abbreviated
Reviewed by Third Party Yes
Expedited Review