FDA 510(k) Application Details - K012028

Device Classification Name	Instrument, Ultrasonic Surgical   More FDA Info for this Device
510(K) Number	K012028
Device Name	Instrument, Ultrasonic Surgical
Applicant	MISONIX, INC. 1938 NEW HIGHWAY FARMINGDALE, NY 11735 US Other 510(k) Applications for this Company
Contact	ALBERT F CLANCY Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LFL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/28/2001
Decision Date	07/27/2001
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review