FDA 510(k) Application Details - K935778

Device Classification Name	Analyzer, Gas, Oxygen, Partial Pressure, Blood-Phase, Indwelling   More FDA Info for this Device
510(K) Number	K935778
Device Name	Analyzer, Gas, Oxygen, Partial Pressure, Blood-Phase, Indwelling
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	868.1200   More FDA Info for this Regulation Number
Classification Product Code	CCE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/03/1993
Decision Date	12/05/1996
Decision	SEKD - SUBST EQUIV - KIT WITH DRUGS
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review