FDA 510(k) Application Details - K092263

Device Classification Name	Ventilator, Continuous, Facility Use   More FDA Info for this Device
510(K) Number	K092263
Device Name	Ventilator, Continuous, Facility Use
Applicant	PROVIDENCE GLOBAL MEDICAL, INC. 4659 SOUTH, 2300 EAST #203 SALT LAKE CITY, UT 84117 US Other 510(k) Applications for this Company
Contact	HELEN REDD 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	07/28/2009
Decision Date	01/21/2010
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