Iq HDL Cholesterol

FDA 510(k) K881891 · Bd Becton Dickinson Vacutainer Systems Preanalytic

Substantially Equivalent

510(k) numberK881891

Submission

Device name
Iq HDL Cholesterol
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic
Franklin Lakes, NJ, US
Received
May 5, 1988
Decision date
June 10, 1988
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 Iq HDL Cholesterol cleared by the FDA?

Iq HDL Cholesterol (K881891) received a 510(k) decision of Substantially Equivalent on June 10, 1988, 36 days after the submission was received.

What is the product code of K881891?

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.