FDA 510(k) Application Details - K241573

Device Classification Name	More FDA Info for this Device
510(K) Number	K241573
Device Name	Alinity m Resp-4-Plex
Applicant	Abbott Molecular Inc 1300 E Touhy Ave Des Plaines, IL 60018 US Other 510(k) Applications for this Company
Contact	Stacy Ferguson Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QOF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/03/2024
Decision Date	02/14/2025
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	MI - Microbiology
Review Advisory Committee	MI - Microbiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review