FDA 510(k) Application Details - K072009

Device Classification Name	Ventilator, Non-Continuous (Respirator)   More FDA Info for this Device
510(K) Number	K072009
Device Name	Ventilator, Non-Continuous (Respirator)
Applicant	WEINMANN GERATE FUR MEDIZIN GMBH + CO. KG KRONSAALSWEG 40 HAMBURG 22525 DE Other 510(k) Applications for this Company
Contact	ECKHARDT ALBERS Other 510(k) Applications for this Contact
Regulation Number	868.5905   More FDA Info for this Regulation Number
Classification Product Code	BZD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/23/2007
Decision Date	12/14/2007
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