FDA 510(k) Application Details - K051889

Device Classification Name	Ventilator, Emergency, Powered (Resuscitator)   More FDA Info for this Device
510(K) Number	K051889
Device Name	Ventilator, Emergency, Powered (Resuscitator)
Applicant	O-TWO MEDICAL TECHNOLOGIES, INC. 7575 KIMBEL ST. MISSISSAUGA, ONTARIO L5S 1C8 CA Other 510(k) Applications for this Company
Contact	AMMAR AL-DOJAILY 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	07/12/2005
Decision Date	08/30/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review