Quikread Whole Blood Hdl-Cholesterol Test Kit

FDA 510(k) K894057 · Photec Diagnostics, Inc.

Substantially Equivalent

510(k) numberK894057

Submission

Device name
Quikread Whole Blood Hdl-Cholesterol Test Kit
Applicant
Photec Diagnostics, Inc.
Mahwah, NJ, US
Received
June 7, 1989
Decision date
August 31, 1989
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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K882307D-ChemJJE · Traditional 08/02/1988SE
K880291Theophylline Test Kit Ref. #A874799LCA · Traditional 03/24/1988SE
K854875Apo-Screen Calibrator & Control Set for HDL Apo A1DER · Traditional 01/24/1986SE
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K853174Apo-Chrome Immunoassay Test Set for ApolipoproteinMSJ · Traditional 08/22/1985SE

Questions and answers

When was Quikread Whole Blood Hdl-Cholesterol Test Kit cleared by the FDA?

Quikread Whole Blood Hdl-Cholesterol Test Kit (K894057) received a 510(k) decision of Substantially Equivalent on August 31, 1989, 85 days after the submission was received.

What is the product code of K894057?

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.