FDA 510(k) Application Details - K960098

Device Classification Name	Cannula, Catheter   More FDA Info for this Device
510(K) Number	K960098
Device Name	Cannula, Catheter
Applicant	RESEARCH MEDICAL, INC. 6864 SOUTH 300 WEST MIDVALE, UT 84047 US Other 510(k) Applications for this Company
Contact	RD HIBBERT Other 510(k) Applications for this Contact
Regulation Number	870.1300   More FDA Info for this Regulation Number
Classification Product Code	DQR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/11/1996
Decision Date	03/26/1996
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