FDA 510(k) Application Details - K102824

Device Classification Name	Ventilator, Emergency, Manual (Resuscitator)   More FDA Info for this Device
510(K) Number	K102824
Device Name	Ventilator, Emergency, Manual (Resuscitator)
Applicant	AMBU A/S 6740 BAYMEADOW DR. GLEN BURNIE, MD 21060 US Other 510(k) Applications for this Company
Contact	SANJAY PARIKH Other 510(k) Applications for this Contact
Regulation Number	868.5915   More FDA Info for this Regulation Number
Classification Product Code	BTM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/29/2010
Decision Date	01/28/2011
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review