Kodak Extachem Clinical Chemistry Slide Digoxin (DGXN)

FDA 510(k) K942610 · Eastman Kodak Company

Substantially Equivalent

510(k) numberK942610

Submission

Device name
Kodak Extachem Clinical Chemistry Slide Digoxin (DGXN)
Applicant
Eastman Kodak Company
Rochester, NY, US
Received
June 2, 1994
Decision date
October 20, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LFM – Enzyme Immunoassay, Digitoxin
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3300
Specialty
Clinical Toxicology

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K954420Axsym DigitoxinLFM · Traditional Abbott Laboratories12/29/1995SE
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K943235Immulite DigitoxinLFM · Traditional Diagnostic Products Corp.10/27/1994SE
K942619Emit 2000 Digoxin Assay/CalibratorsLFM · Traditional Syva Co.09/20/1994SE
K915465Digitoxin Fpia Reagent SetLFM · Traditional Sigma Diagnostics, Inc.01/27/1992SE

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Questions and answers

When was Kodak Extachem Clinical Chemistry Slide Digoxin (DGXN) cleared by the FDA?

Kodak Extachem Clinical Chemistry Slide Digoxin (DGXN) (K942610) received a 510(k) decision of Substantially Equivalent on October 20, 1994, 140 days after the submission was received.

What is the product code of K942610?

The FDA product code is LFM – Enzyme Immunoassay, Digitoxin, a Class II (moderate risk) device regulated under 21 CFR 862.3300.