FDA 510(k) Application Details - K990366

Device Classification Name	Instrument, Ent Manual Surgical   More FDA Info for this Device
510(K) Number	K990366
Device Name	Instrument, Ent Manual Surgical
Applicant	EXMOOR PLASTICS LTD. LISIEUX WAY TAUNTON, SOMERSET TA1 2LB GB Other 510(k) Applications for this Company
Contact	MARGARET BLACKMORE Other 510(k) Applications for this Contact
Regulation Number	874.4420   More FDA Info for this Regulation Number
Classification Product Code	LRC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/05/1999
Decision Date	03/05/1999
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