FDA 510(k) Application Details - K231465

Device Classification Name	Assay, Glycosylated Hemoglobin   More FDA Info for this Device
510(K) Number	K231465
Device Name	Assay, Glycosylated Hemoglobin
Applicant	Qurasense 3517 Edison Way, Ste. D Menlo Park, CA 94025 US Other 510(k) Applications for this Company
Contact	Sara Naseri Other 510(k) Applications for this Contact
Regulation Number	864.7470   More FDA Info for this Regulation Number
Classification Product Code	LCP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/19/2023
Decision Date	12/06/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HE - Hematology
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review