Lipase Hydrolysis/Glycerol Kinase, Triglycerides

FDA 510(k) K863874 · Electro-Nucleonics Laboratories, Inc.

Substantially Equivalent

510(k) numberK863874

Submission

Device name
Lipase Hydrolysis/Glycerol Kinase, Triglycerides
Applicant
Electro-Nucleonics Laboratories, Inc.
Columbia, MD, US
Received
October 3, 1986
Decision date
November 13, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CDT – Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides
Device class
Class I (low risk)
Regulation
21 CFR 862.1705
Specialty
Clinical Chemistry

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K870928Cholesterol (Total) Analysis ProductsCHH · Traditional 04/22/1987SE
K862640Amylase LTSCJA · Traditional 09/09/1986SE
K853372Gemstar Ipa Theophylline Test KitKLS · Traditional 09/04/1985SE
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Questions and answers

When was Lipase Hydrolysis/Glycerol Kinase, Triglycerides cleared by the FDA?

Lipase Hydrolysis/Glycerol Kinase, Triglycerides (K863874) received a 510(k) decision of Substantially Equivalent on November 13, 1986, 41 days after the submission was received.

What is the product code of K863874?

The FDA product code is CDT – Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides, a Class I (low risk) device regulated under 21 CFR 862.1705.