FDA 510(k) Application Details - K230173

Device Classification Name	Ventilator, Continuous, Minimal Ventilatory Support,Facility Use   More FDA Info for this Device
510(K) Number	K230173
Device Name	Ventilator, Continuous, Minimal Ventilatory Support,Facility Use
Applicant	Maquet Critical Care AB Rontgenvagen 2 Solna SE-171 54 SE Other 510(k) Applications for this Company
Contact	David Ardanius Other 510(k) Applications for this Contact
Regulation Number	868.5895   More FDA Info for this Regulation Number
Classification Product Code	MNT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/20/2023
Decision Date	07/06/2023
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