Raichem HDL Cholesterol Using Cantrol HDL Precipitating Tubes on the Cobas Mira Anaylzer

FDA 510(k) K023784 · Hemagen Diagnostics, Inc.

Substantially Equivalent

510(k) numberK023784

Submission

Device name
Raichem HDL Cholesterol Using Cantrol HDL Precipitating Tubes on the Cobas Mira Anaylzer
Applicant
Hemagen Diagnostics, Inc.
Columbia, MD, US
Received
November 12, 2002
Decision date
December 24, 2002
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
LBR – Ldl & Vldl Precipitation, Hdl
Device class
Class I (low risk)
Regulation
21 CFR 862.1475
Specialty
Clinical Chemistry

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Questions and answers

When was Raichem HDL Cholesterol Using Cantrol HDL Precipitating Tubes on the Cobas Mira Anaylzer cleared by the FDA?

Raichem HDL Cholesterol Using Cantrol HDL Precipitating Tubes on the Cobas Mira Anaylzer (K023784) received a 510(k) decision of Substantially Equivalent on December 24, 2002, 42 days after the submission was received.

What is the product code of K023784?

The FDA product code is LBR – Ldl & Vldl Precipitation, Hdl, a Class I (low risk) device regulated under 21 CFR 862.1475.