FDA 510(k) Application Details - K151814

Device Classification Name	Ventilator, Continuous, Facility Use   More FDA Info for this Device
510(K) Number	K151814
Device Name	Ventilator, Continuous, Facility Use
Applicant	MAQUET CRITICAL CARE AB RONTGENVAGEN 2 SOLNA SE-171 54 SE Other 510(k) Applications for this Company
Contact	MARIA VON BAHR 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	07/06/2015
Decision Date	12/21/2015
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