FDA 510(k) Application Details - K140054

Device Classification Name	Ventilator, Non-Continuous (Respirator)   More FDA Info for this Device
510(K) Number	K140054
Device Name	Ventilator, Non-Continuous (Respirator)
Applicant	RESMED LTD 9001 SPECTRUM CENTER BOULEVARD SAN DIEGO, CA 92123 US Other 510(k) Applications for this Company
Contact	JIM CASSI 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	01/09/2014
Decision Date	05/16/2014
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