FDA 510(k) Application Details - K223710

Device Classification Name	Glucose Oxidase, Glucose   More FDA Info for this Device
510(K) Number	K223710
Device Name	Glucose Oxidase, Glucose
Applicant	Abbott Point of Care Inc. 400 College Road East Princeton, NJ 08540 US Other 510(k) Applications for this Company
Contact	Jacquelyn Gesumaria Other 510(k) Applications for this Contact
Regulation Number	862.1345   More FDA Info for this Regulation Number
Classification Product Code	CGA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/12/2022
Decision Date	07/28/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review