FDA 510(k) Application Details - K933841

Device Classification Name	Powered Laser Surgical Instrument   More FDA Info for this Device
510(K) Number	K933841
Device Name	Powered Laser Surgical Instrument
Applicant	PREMIER LASER SYSTEMS, INC. 3 MORGAN IRVINE, CA 92718 US Other 510(k) Applications for this Company
Contact	COLLETE COZEAN 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	08/04/1993
Decision Date	05/05/1997
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