FDA 510(k) Application Details - K233618

Device Classification Name	Device, Sleep Assessment   More FDA Info for this Device
510(K) Number	K233618
Device Name	Device, Sleep Assessment
Applicant	Oxehealth Limited Magdalen Centre North Oxford Science Park Oxford OX4 4GA GB Other 510(k) Applications for this Company
Contact	Joao Jorge Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LEL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/13/2023
Decision Date	04/03/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	NE - Neurology
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review