FDA 510(k) Application Details - K983940

Device Classification Name	Introducer, Catheter   More FDA Info for this Device
510(K) Number	K983940
Device Name	Introducer, Catheter
Applicant	ADAM SPENCE CORP. 1746 RT. 34 P.O. BOX 1467 WALL, NJ 07719 US Other 510(k) Applications for this Company
Contact	CAROL ROSENBLOOM 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	11/05/1998
Decision Date	07/15/1999
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