510(k) K020575

ATAC DIRECT LDL REAGENT AND ATAC DIRECT LDL CALIBRATOR KITS by Elan Diagnostics — Product Code MRR

K020575 is an FDA 510(k) premarket notification submitted by Elan Diagnostics for the device "ATAC DIRECT LDL REAGENT AND ATAC DIRECT LDL CALIBRATOR KITS". The FDA issued a decision of Substantially Equivalent on April 12, 2002. The device falls under product code MRR (System, Test, Low Density, Lipoprotein), a Class I device regulated under 21 CFR 862.1475. Elan Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 12, 2002
Date Received
February 21, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Test, Low Density, Lipoprotein
Device Class
Class I
Regulation Number
862.1475
Review Panel
CH
Submission Type