510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K050823Substantially Equivalent

Direct Hdl Cholesterol and Direct Hdl/ldl Calibrator

Teco Diagnostics, Anaheim CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K050823 is the FDA 510(k) clearance record for DIRECT HDL CHOLESTEROL AND DIRECT HDL/LDL CALIBRATOR, a class I device, cleared for Teco Diagnostics on under FDA product code LBR (Ldl & Vldl Precipitation, Hdl). FDA records list 55 510(k) clearances for Teco Diagnostics, from to . As of , FDA records show no recalls naming K050823.

Clearance record

Decision date
Received
(117 days to decision)
Product code
LBR Ldl & Vldl Precipitation, Hdl
Regulation
21 CFR 862.1475
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Teco Diagnostics 1268 N Lakeview Ave., Anaheim CA
510(k) summary
Statement
Third party review
No

Clearances, product code LBR

Trailing 12 months

FDA records hold no clearances under product code LBR in the trailing twelve months.

FDA records show no clearances under product code LBR in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LBR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260