HDL Cholesterol Reagent (PTA/MGCL2)

FDA 510(k) K890023 · Sigma Diagnostics, Inc.

Substantially Equivalent

510(k) numberK890023

Submission

Device name
HDL Cholesterol Reagent (PTA/MGCL2)
Applicant
Sigma Diagnostics, Inc.
St. Louis, MO, US
Received
January 4, 1989
Decision date
February 17, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LBR – Ldl & Vldl Precipitation, Hdl
Device class
Class I (low risk)
Regulation
21 CFR 862.1475
Specialty
Clinical Chemistry

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K992029Atac Direct HDL Cholesterol Reagent and Atac Hdl-C Calibrator KitsLBR · Traditional Elan Diagnostics08/12/1999SE
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Questions and answers

When was HDL Cholesterol Reagent (PTA/MGCL2) cleared by the FDA?

HDL Cholesterol Reagent (PTA/MGCL2) (K890023) received a 510(k) decision of Substantially Equivalent on February 17, 1989, 44 days after the submission was received.

What is the product code of K890023?

The FDA product code is LBR – Ldl & Vldl Precipitation, Hdl, a Class I (low risk) device regulated under 21 CFR 862.1475.