FDA 510(k) Application Details - K173193

Device Classification Name	Ventilator, Non-Continuous (Respirator)   More FDA Info for this Device
510(K) Number	K173193
Device Name	Ventilator, Non-Continuous (Respirator)
Applicant	Fisher & Paykel Healthcare Ltd 15 Maurice Paykel Place East Tamaki 2013 NZ Other 510(k) Applications for this Company
Contact	Jayanti Karandikar 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	10/02/2017
Decision Date	08/08/2018
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