FDA 510(k) Application Details - K213098

Device Classification Name	Ventilator, Continuous, Facility Use   More FDA Info for this Device
510(K) Number	K213098
Device Name	Ventilator, Continuous, Facility Use
Applicant	Origin Medical Devices 23 Corporate Plaza Newport Beach, CA 92660 US Other 510(k) Applications for this Company
Contact	Brent Chamblee 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	09/24/2021
Decision Date	07/20/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review