510(k) K050823

DIRECT HDL CHOLESTEROL AND DIRECT HDL/LDL CALIBRATOR by Teco Diagnostics — Product Code LBR

K050823 is an FDA 510(k) premarket notification submitted by Teco Diagnostics for the device "DIRECT HDL CHOLESTEROL AND DIRECT HDL/LDL CALIBRATOR". The FDA issued a decision of Substantially Equivalent on July 26, 2005. The device falls under product code LBR (Ldl & Vldl Precipitation, Hdl), 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
July 26, 2005
Date Received
March 31, 2005
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ldl & Vldl Precipitation, Hdl
Device Class
Class I
Regulation Number
862.1475
Review Panel
CH
Submission Type