FDA 510(k) Application Details - K962307

Device Classification Name	Catheter, Electrode Recording, Or Probe, Electrode Recording   More FDA Info for this Device
510(K) Number	K962307
Device Name	Catheter, Electrode Recording, Or Probe, Electrode Recording
Applicant	FIDUS MEDICAL TECHNOLOGY CORP. 47929 FREMONT BLVD. FREMONT, CA 94538 US Other 510(k) Applications for this Company
Contact	TED ORMSBY Other 510(k) Applications for this Contact
Regulation Number	870.1220   More FDA Info for this Regulation Number
Classification Product Code	DRF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/17/1996
Decision Date	09/17/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review