Barbiturate Enzyme Immunoassay Kit

FDA 510(k) K882663 · General Diagnostics

Substantially Equivalent

510(k) numberK882663

Submission

Device name
Barbiturate Enzyme Immunoassay Kit
Applicant
General Diagnostics
Great Neck, NY, US
Received
June 27, 1988
Decision date
September 19, 1988
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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Questions and answers

When was Barbiturate Enzyme Immunoassay Kit cleared by the FDA?

Barbiturate Enzyme Immunoassay Kit (K882663) received a 510(k) decision of Substantially Equivalent on September 19, 1988, 84 days after the submission was received.

What is the product code of K882663?

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