Cholesterol Kit, Hdl-Ds

FDA 510(k) K790553 · Beckman Instruments, Inc.

Substantially Equivalent

510(k) numberK790553

Submission

Device name
Cholesterol Kit, Hdl-Ds
Applicant
Beckman Instruments, Inc.
Mchenry, IL, US
Received
March 19, 1979
Decision date
June 15, 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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Questions and answers

When was Cholesterol Kit, Hdl-Ds cleared by the FDA?

Cholesterol Kit, Hdl-Ds (K790553) received a 510(k) decision of Substantially Equivalent on June 15, 1979, 88 days after the submission was received.

What is the product code of K790553?

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.