FDA 510(k) Application Details - K233555

Device Classification Name	Ventilator, Non-Continuous (Respirator)   More FDA Info for this Device
510(K) Number	K233555
Device Name	Ventilator, Non-Continuous (Respirator)
Applicant	Philips Respironics 1001 Murry Ridge Ln Murrysville, PA 15668 US Other 510(k) Applications for this Company
Contact	Emily Tobin 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	11/06/2023
Decision Date	07/31/2024
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