Direct LDL Cholesterol Liquid Color and Stanbio Direct Hdl/Ldl Cholesterol Calibrator

FDA 510(k) K032936 · Stanbio Laboratory

Substantially Equivalent

510(k) numberK032936

Submission

Device name
Direct LDL Cholesterol Liquid Color and Stanbio Direct Hdl/Ldl Cholesterol Calibrator
Applicant
Stanbio Laboratory
Boerne, TX, US
Received
September 22, 2003
Decision date
March 12, 2004
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JIX – Calibrator, Multi-Analyte Mixture
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1150
Specialty
Clinical Chemistry

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Questions and answers

When was Direct LDL Cholesterol Liquid Color and Stanbio Direct Hdl/Ldl Cholesterol Calibrator cleared by the FDA?

Direct LDL Cholesterol Liquid Color and Stanbio Direct Hdl/Ldl Cholesterol Calibrator (K032936) received a 510(k) decision of Substantially Equivalent on March 12, 2004, 172 days after the submission was received.

What is the product code of K032936?

The FDA product code is JIX – Calibrator, Multi-Analyte Mixture, a Class II (moderate risk) device regulated under 21 CFR 862.1150.