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FDA 510(k) Application Details - K030508
Device Classification Name
Powered Laser Surgical Instrument
More FDA Info for this Device
510(K) Number
K030508
Device Name
Powered Laser Surgical Instrument
Applicant
DEPILASE GROUP LTD.
ONE CANADA SQUARE
CANARY WHARF
LONDON E14 5DY GB
Other 510(k) Applications for this Company
Contact
MARIO LUCA RUSSO
Other 510(k) Applications for this Contact
Regulation Number
878.4810
More FDA Info for this Regulation Number
Classification Product Code
GEX
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/19/2003
Decision Date
05/20/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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