Quali. Enzyme Immuno. of Barbiturates in Urine

FDA 510(k) K864993 · General Diagnostics

Substantially Equivalent

510(k) numberK864993

Submission

Device name
Quali. Enzyme Immuno. of Barbiturates in Urine
Applicant
General Diagnostics
Great Neck, NY, US
Received
December 22, 1986
Decision date
March 31, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DIS – Enzyme Immunoassay, Barbiturate
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3150
Specialty
Clinical Toxicology

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More from Phamatech, Inc.

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K871305Cocaine Metabolite Enzyme Immunoassay KitDIO · Traditional 06/05/1987SE
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K833709Ceftizoxime 30 MCG Antimicrobial DiskJTN · Traditional 12/30/1983SE
K832653Cefuroxime 30MCG. Suscep DiskJTN · Traditional 10/14/1983SE
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Questions and answers

When was Quali. Enzyme Immuno. of Barbiturates in Urine cleared by the FDA?

Quali. Enzyme Immuno. of Barbiturates in Urine (K864993) received a 510(k) decision of Substantially Equivalent on March 31, 1987, 99 days after the submission was received.

What is the product code of K864993?

The FDA product code is DIS – Enzyme Immunoassay, Barbiturate, a Class II (moderate risk) device regulated under 21 CFR 862.3150.