Dade High Density Lipoprotein Cholestero

FDA 510(k) K792183 · Dade, Baxter Travenol Diagnostics, Inc.

Substantially Equivalent

510(k) numberK792183

Submission

Device name
Dade High Density Lipoprotein Cholestero
Applicant
Dade, Baxter Travenol Diagnostics, Inc.
Mchenry, IL, US
Received
October 29, 1979
Decision date
November 13, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LBS – Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl
Device class
Class I (low risk)
Regulation
21 CFR 862.1475
Specialty
Clinical Chemistry

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K791922Harleco Brand Clinicard Lipase Test SetCET · Traditional 11/27/1979SE
K790776Dade Low Ionic Strength Soluition (Liss)KSG · Traditional 05/23/1979SE
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Questions and answers

When was Dade High Density Lipoprotein Cholestero cleared by the FDA?

Dade High Density Lipoprotein Cholestero (K792183) received a 510(k) decision of Substantially Equivalent on November 13, 1979, 15 days after the submission was received.

What is the product code of K792183?

The FDA product code is LBS – Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl, a Class I (low risk) device regulated under 21 CFR 862.1475.