FDA 510(k) Application Details - K030598

Device Classification Name	Scalpel, Ultrasonic, Reprocessed   More FDA Info for this Device
510(K) Number	K030598
Device Name	Scalpel, Ultrasonic, Reprocessed
Applicant	MEDISISS 723 CURTIS COURT PO BOX 2060 SISTERS, OR 97759 US Other 510(k) Applications for this Company
Contact	MARY ANN BARKER 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	02/25/2003
Decision Date	01/23/2004
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