FDA 510(k) Application Details - K222207

Device Classification Name	Ventilator, Continuous, Facility Use   More FDA Info for this Device
510(K) Number	K222207
Device Name	Ventilator, Continuous, Facility Use
Applicant	Draegerwerk AG & CO KGaA 53/55 Moislinger Allee Luebeck 23542 DE Other 510(k) Applications for this Company
Contact	Nataliia Semenova 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	07/25/2022
Decision Date	05/16/2023
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