Olympus Lactate Dehydrogenase Reagent

FDA 510(k) K923412 · Olympus Corp.

Substantially Equivalent

510(k) numberK923412

Submission

Device name
Olympus Lactate Dehydrogenase Reagent
Applicant
Olympus Corp.
Lake Success, NY, US
Received
July 10, 1992
Decision date
September 18, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
CFJ – Nad Reduction/Nadh Oxidation, Lactate Dehydrogenase
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1440
Specialty
Clinical Chemistry

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K971398Ld-L ReagentCFJ · Traditional Carolina Liquid Chemistries Corp.05/02/1997SE
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K961431Lactate Dehydrogenase Reagent SetCFJ · Traditional Pointe Scientific, Inc.,06/03/1996SE
K952747Lactate Dehydrogenase Reagent SystemCFJ · Traditional Medical Diagnostic Technologies, Inc.08/07/1995SE

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Questions and answers

When was Olympus Lactate Dehydrogenase Reagent cleared by the FDA?

Olympus Lactate Dehydrogenase Reagent (K923412) received a 510(k) decision of Substantially Equivalent on September 18, 1992, 70 days after the submission was received.

What is the product code of K923412?

The FDA product code is CFJ – Nad Reduction/Nadh Oxidation, Lactate Dehydrogenase, a Class II (moderate risk) device regulated under 21 CFR 862.1440.