FDA 510(k) Application Details - K982540

Device Classification Name	Catheter,Intracardiac Mapping,High-Density Array   More FDA Info for this Device
510(K) Number	K982540
Device Name	Catheter,Intracardiac Mapping,High-Density Array
Applicant	CARDIAC PATHWAYS CORP. 995 BENECIA AVE. SUNNYVALE, CA 94086 US Other 510(k) Applications for this Company
Contact	ERIN DIGNAN Other 510(k) Applications for this Contact
Regulation Number	870.1220   More FDA Info for this Regulation Number
Classification Product Code	MTD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/21/1998
Decision Date	01/27/1999
Decision	SESU - SE - WITH LIMITATIONS
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review