FDA 510(k) Application Details - K960937

Device Classification Name	Cpb Check Valve, Retrograde Flow, In-Line   More FDA Info for this Device
510(K) Number	K960937
Device Name	Cpb Check Valve, Retrograde Flow, In-Line
Applicant	R D INTL. 304 ARBORCREST RICHARDSON, TX 75080 US Other 510(k) Applications for this Company
Contact	MIKE DAVIS Other 510(k) Applications for this Contact
Regulation Number	870.4400   More FDA Info for this Regulation Number
Classification Product Code	MJJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/08/1996
Decision Date	06/05/1996
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