FDA 510(k) Application Details - K223679

Device Classification Name	More FDA Info for this Device
510(K) Number	K223679
Device Name	Access AMH
Applicant	Beckman Coulter Inc 1000 Lake Hazeltine Drive Chaska, MN 55318 US Other 510(k) Applications for this Company
Contact	Kate Oelberg Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	PQO Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/08/2022
Decision Date	02/03/2023
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