Cocaine Dipstick Test, Model D747-A

FDA 510(k) K010239 · Teco Diagnostics

Substantially Equivalent

510(k) numberK010239

Submission

Device name
Cocaine Dipstick Test, Model D747-A
Applicant
Teco Diagnostics
Anaheim, CA, US
Received
January 25, 2001
Decision date
June 25, 2001
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
DIO – Enzyme Immunoassay, Cocaine And Cocaine Metabolites
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3250
Specialty
Clinical Toxicology

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Questions and answers

When was Cocaine Dipstick Test, Model D747-A cleared by the FDA?

Cocaine Dipstick Test, Model D747-A (K010239) received a 510(k) decision of Substantially Equivalent on June 25, 2001, 151 days after the submission was received.

What is the product code of K010239?

The FDA product code is DIO – Enzyme Immunoassay, Cocaine And Cocaine Metabolites, a Class II (moderate risk) device regulated under 21 CFR 862.3250.