FDA 510(k) Application Details - K043358

Device Classification Name	Scalpel, Ultrasonic, Reprocessed   More FDA Info for this Device
510(K) Number	K043358
Device Name	Scalpel, Ultrasonic, Reprocessed
Applicant	ALLIANCE MEDICAL CORP. 10232 SOUTH 51ST ST. PHOENIX, AZ 85044 US Other 510(k) Applications for this Company
Contact	ELIZABETH RENKEN Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	NLQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/06/2004
Decision Date	06/06/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review