FDA 510(k) Application Details - K241800

Device Classification Name	System, Test, Low Density, Lipoprotein   More FDA Info for this Device
510(K) Number	K241800
Device Name	System, Test, Low Density, Lipoprotein
Applicant	Siemens Healthcare Diagnostics, Inc. 500 GBC Drive P.O. Box 6101 Newark, DE 19711 US Other 510(k) Applications for this Company
Contact	Justin Thomas Other 510(k) Applications for this Contact
Regulation Number	862.1475   More FDA Info for this Regulation Number
Classification Product Code	MRR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/21/2024
Decision Date	07/26/2024
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