Piccolo HDL Test System

FDA 510(k) K023640 · Abaxis, Inc.

Substantially Equivalent

510(k) numberK023640

Submission

Device name
Piccolo HDL Test System
Applicant
Abaxis, Inc.
Union City, CA, US
Received
October 30, 2002
Decision date
January 24, 2003
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 Piccolo HDL Test System cleared by the FDA?

Piccolo HDL Test System (K023640) received a 510(k) decision of Substantially Equivalent on January 24, 2003, 86 days after the submission was received.

What is the product code of K023640?

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.