FDA 510(k) Application Details - K974142

Device Classification Name	Powered Laser Surgical Instrument   More FDA Info for this Device
510(K) Number	K974142
Device Name	Powered Laser Surgical Instrument
Applicant	AMERICAN LASERS, INC. 808 NORTH HILL ST. ATTN: DAVID K. QUON, MD/PRES. LOS ANGELES, CA 90011 US Other 510(k) Applications for this Company
Contact	DAVID K QUON 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	11/03/1997
Decision Date	01/28/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review