FDA 510(k) Application Details - K223573

Device Classification Name	Ventilatory Effort Recorder   More FDA Info for this Device
510(K) Number	K223573
Device Name	Ventilatory Effort Recorder
Applicant	Onera B.V. Torenallee 42-54 Eindhoven 5617BD NL Other 510(k) Applications for this Company
Contact	Ruben de Francisco Martin Other 510(k) Applications for this Contact
Regulation Number	868.2375   More FDA Info for this Regulation Number
Classification Product Code	MNR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/30/2022
Decision Date	08/18/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review