Sigms Proced. 228 UV Lactate Dehydro

FDA 510(k) K841917 · Sigma Diagnostics, Inc.

Substantially Equivalent

510(k) numberK841917

Submission

Device name
Sigms Proced. 228 UV Lactate Dehydro
Applicant
Sigma Diagnostics, Inc.
Mchenry, IL, US
Received
May 9, 1984
Decision date
June 14, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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Questions and answers

When was Sigms Proced. 228 UV Lactate Dehydro cleared by the FDA?

Sigms Proced. 228 UV Lactate Dehydro (K841917) received a 510(k) decision of Substantially Equivalent on June 14, 1984, 36 days after the submission was received.

What is the product code of K841917?

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