FDA 510(k) Application Details - K962978

Device Classification Name	Introducer, Catheter   More FDA Info for this Device
510(K) Number	K962978
Device Name	Introducer, Catheter
Applicant	JOHNSON & JOHNSON MEDICAL, INC. 1350 WILLOW RD. MENLO PARK, CA 94025 US Other 510(k) Applications for this Company
Contact	PHYLLIS ELSON Other 510(k) Applications for this Contact
Regulation Number	870.1340   More FDA Info for this Regulation Number
Classification Product Code	DYB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/31/1996
Decision Date	01/07/1997
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