HDL Cholesterol Reagent, Model 10211

FDA 510(k) K073497 · Medica Corp.

Substantially Equivalent

510(k) numberK073497

Submission

Device name
HDL Cholesterol Reagent, Model 10211
Applicant
Medica Corp.
Bedford, MA, US
Received
December 13, 2007
Decision date
April 14, 2008
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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 HDL Cholesterol Reagent, Model 10211 cleared by the FDA?

HDL Cholesterol Reagent, Model 10211 (K073497) received a 510(k) decision of Substantially Equivalent on April 14, 2008, 123 days after the submission was received.

What is the product code of K073497?

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.