FDA 510(k) Application Details - K083688

Device Classification Name	Ventilator, Continuous, Facility Use   More FDA Info for this Device
510(K) Number	K083688
Device Name	Ventilator, Continuous, Facility Use
Applicant	PULMONETIC SYSTEMS, INC. 17400 MEDINA ROAD SUITE 100 MINNEAPOLIS, MN 55447 US Other 510(k) Applications for this Company
Contact	ROBERT C SAMEC 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	12/12/2008
Decision Date	03/18/2009
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