FDA 510(k) Application Details - K032601

Device Classification Name	Generator, Lesion, Radiofrequency   More FDA Info for this Device
510(K) Number	K032601
Device Name	Generator, Lesion, Radiofrequency
Applicant	VALLEY FORGE SCIENTIFIC CORP. 136 GREEN TREE RD. OAKS, PA 19456 US Other 510(k) Applications for this Company
Contact	JERRY MALIS Other 510(k) Applications for this Contact
Regulation Number	882.4400   More FDA Info for this Regulation Number
Classification Product Code	GXD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/25/2003
Decision Date	04/01/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review