FDA 510(k) Application Details - K163127

Device Classification Name	Ventilator, Continuous, Facility Use   More FDA Info for this Device
510(K) Number	K163127
Device Name	Ventilator, Continuous, Facility Use
Applicant	IMTMEDICAL AG GEWERBESTRASSE 8 BUCHS SG CH-9470 CH Other 510(k) Applications for this Company
Contact	BEAT KELLER 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	11/08/2016
Decision Date	07/31/2017
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