FDA 510(k) Application Details - K082724

Device Classification Name	Ventilator, Continuous, Facility Use   More FDA Info for this Device
510(K) Number	K082724
Device Name	Ventilator, Continuous, Facility Use
Applicant	NEWPORT MEDICAL INSTRUMENTS, INC. 1620 SUNFLOWER AVE. COSTA MESA, CA 92626 US Other 510(k) Applications for this Company
Contact	DIANA RODRIGUEZ Other 510(k) Applications for this Contact
Regulation Number	868.5895   More FDA Info for this Regulation Number
Classification Product Code	CBK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/17/2008
Decision Date	12/16/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review