FDA 510(k) Application Details - K083730

Device Classification Name	Powered Laser Surgical Instrument   More FDA Info for this Device
510(K) Number	K083730
Device Name	Powered Laser Surgical Instrument
Applicant	AESTHERA CORPORATION 1070 CONCORD AVE SUITE 230 CONCORD, CA 94520 US Other 510(k) Applications for this Company
Contact	PAMELA M BUCKMAN 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	12/16/2008
Decision Date	01/09/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review