FDA 510(k) Application Details - K981041

Device Classification Name	Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece   More FDA Info for this Device
510(K) Number	K981041
Device Name	Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
Applicant	SURGICAL LASER TECHNOLOGIES, INC. 147 KEYSTONE DR. MONTGOMERYVILLE, PA 18936 US Other 510(k) Applications for this Company
Contact	MONICA FERRANTE Other 510(k) Applications for this Contact
Regulation Number	874.4250   More FDA Info for this Regulation Number
Classification Product Code	ERL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/20/1998
Decision Date	08/27/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	EN - Ear, Nose, & Throat
Review Advisory Committee	EN - Ear, Nose, & Throat
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review