FDA 510(k) Application Details - K132021

Device Classification Name	Ventilator, Emergency, Powered (Resuscitator)   More FDA Info for this Device
510(K) Number	K132021
Device Name	Ventilator, Emergency, Powered (Resuscitator)
Applicant	ALLIED HEALTHCARE PRODUCTS, INC. 1720 SUBLETTE AVE. Saint Louis, MO 63110 US Other 510(k) Applications for this Company
Contact	STEPHEN MUNDWILLER Other 510(k) Applications for this Contact
Regulation Number	868.5925   More FDA Info for this Regulation Number
Classification Product Code	BTL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/02/2013
Decision Date	04/02/2014
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review