FDA 510(k) Application Details - K951739

Device Classification Name	Pump, Infusion, Analytical Sampling   More FDA Info for this Device
510(K) Number	K951739
Device Name	Pump, Infusion, Analytical Sampling
Applicant	VIA MEDICAL CORP. 11425 SORRENTO VALLEY RD. SAN DIEGO, CA 92121 US Other 510(k) Applications for this Company
Contact	DAN MCKAY Other 510(k) Applications for this Contact
Regulation Number	880.5725   More FDA Info for this Regulation Number
Classification Product Code	LZF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/14/1995
Decision Date	02/28/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review