510(k) K051121

DIRECT LDL CHOLESTEROL, MODEL L530-60H by Teco Diagnostics — Product Code MRR

K051121 is an FDA 510(k) premarket notification submitted by Teco Diagnostics for the device "DIRECT LDL CHOLESTEROL, MODEL L530-60H". The FDA issued a decision of Substantially Equivalent on August 8, 2005. The device falls under product code MRR (System, Test, Low Density, Lipoprotein), a Class I device regulated under 21 CFR 862.1475. Teco Diagnostics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 8, 2005
Date Received
May 2, 2005
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