FDA 510(k) Application Details - K990780

Device Classification Name	Powered Laser Surgical Instrument   More FDA Info for this Device
510(K) Number	K990780
Device Name	Powered Laser Surgical Instrument
Applicant	AMERICAN LASER MEDICAL 1832 SOUTH 3850 WEST SALT LAKE CITY, UT 84104 US Other 510(k) Applications for this Company
Contact	DANIEL HOEFER 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	03/09/1999
Decision Date	03/22/1999
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