FDA 510(k) Application Details - K240601

Device Classification Name	Oximeter, Tissue Saturation   More FDA Info for this Device
510(K) Number	K240601
Device Name	Oximeter, Tissue Saturation
Applicant	Kent Imaging Inc Suite 300, 1210 8 Street SW Calgary T2R 1L3 CA Other 510(k) Applications for this Company
Contact	Hitalo Arume Other 510(k) Applications for this Contact
Regulation Number	870.2700   More FDA Info for this Regulation Number
Classification Product Code	MUD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/04/2024
Decision Date	04/02/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	Y
Expedited Review