FDA 510(k) Application Details - K971619

Device Classification Name	Catheter, Continuous Flush   More FDA Info for this Device
510(K) Number	K971619
Device Name	Catheter, Continuous Flush
Applicant	E-MED CORP. 651 CAMPUS DR. ST. PAUL, MN 55112 US Other 510(k) Applications for this Company
Contact	JOHN DOCKTER Other 510(k) Applications for this Contact
Regulation Number	870.1210   More FDA Info for this Regulation Number
Classification Product Code	KRA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/01/1997
Decision Date	02/27/1998
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