V-Trend Dig Enzyme Immunoassay Test Kit

FDA 510(k) K854972 · V-Tech, Inc.

Substantially Equivalent

510(k) numberK854972

Submission

Device name
V-Trend Dig Enzyme Immunoassay Test Kit
Applicant
V-Tech, Inc.
Pomona, CA, US
Received
December 11, 1985
Decision date
January 22, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KXT – Enzyme Immunoassay, Digoxin
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3320
Specialty
Clinical Toxicology

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Questions and answers

When was V-Trend Dig Enzyme Immunoassay Test Kit cleared by the FDA?

V-Trend Dig Enzyme Immunoassay Test Kit (K854972) received a 510(k) decision of Substantially Equivalent on January 22, 1986, 42 days after the submission was received.

What is the product code of K854972?

The FDA product code is KXT – Enzyme Immunoassay, Digoxin, a Class II (moderate risk) device regulated under 21 CFR 862.3320.