DGTX Flex Reagent Cartridge, Model DF36

FDA 510(k) K990251 · Dade Behring, Inc.

Substantially Equivalent

510(k) numberK990251

Submission

Device name
DGTX Flex Reagent Cartridge, Model DF36
Applicant
Dade Behring, Inc.
Newark, DE, US
Received
January 27, 1999
Decision date
March 31, 1999
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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K943235Immulite DigitoxinLFM · Traditional Diagnostic Products Corp.10/27/1994SE
K942610Kodak Extachem Clinical Chemistry Slide Digoxin (DGXN)LFM · Traditional Eastman Kodak Company10/20/1994SE
K942619Emit 2000 Digoxin Assay/CalibratorsLFM · Traditional Syva Co.09/20/1994SE
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Questions and answers

When was DGTX Flex Reagent Cartridge, Model DF36 cleared by the FDA?

DGTX Flex Reagent Cartridge, Model DF36 (K990251) received a 510(k) decision of Substantially Equivalent on March 31, 1999, 63 days after the submission was received.

What is the product code of K990251?

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