HDL Cholesterol, Product No's 124-01, CH102-01

FDA 510(k) K991665 · A.P. Total Care, Inc.

Substantially Equivalent

510(k) numberK991665

Submission

Device name
HDL Cholesterol, Product No's 124-01, CH102-01
Applicant
A.P. Total Care, Inc.
Bridgeport, CT, US
Received
May 14, 1999
Decision date
August 10, 1999
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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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K991664LDL Cholesterol, Product No's, 124-01, CH102-01LBS · Traditional 08/19/1999SE
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K991870Electrolytes (Na+, K+, Cl-), Product No's 114-01, 114-02, 114-03CGZ · Traditional 07/30/1999SE
K991666Tibc, Product No's 123-0, 123-02, FE109-01, FE109-02JMO · Traditional 06/30/1999SE
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Questions and answers

When was HDL Cholesterol, Product No's 124-01, CH102-01 cleared by the FDA?

HDL Cholesterol, Product No's 124-01, CH102-01 (K991665) received a 510(k) decision of Substantially Equivalent on August 10, 1999, 88 days after the submission was received.

What is the product code of K991665?

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.