Il Test(Tm) Benzodiazepine

FDA 510(k) K914815 · Instrumentation Laboratory CO

Substantially Equivalent

510(k) numberK914815

Submission

Device name
Il Test(Tm) Benzodiazepine
Applicant
Instrumentation Laboratory CO
Lexington, MA, US
Received
October 25, 1991
Decision date
January 27, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JXM – Enzyme Immunoassay, Benzodiazepine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3170
Specialty
Clinical Toxicology

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K163590Psychemedics Microplate EIA for Benzodiazepines in HairJXM · Traditional Psychemedics Corporation09/15/2017SE
K163704Healgen Multi-Drug Urine Test Cup; Healgen Multi-Drug Urine Test Dip CardJXM · Special Healgen Scientific,, LLC08/02/2017SE
K153597Healgen Multi-Drug Urine Test Cup, Healgen Multi-Drug Urine Test Dip CardJXM · Special Healgen Scientific,, LLC05/23/2016SE
K151771Immunalysis Benzodiazepines Urine Enzyme Immunoassay, Immunalysis Multi-Drug CalibratorsJXM · Traditional Immunalysis Corporation01/05/2016SE
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Questions and answers

When was Il Test(Tm) Benzodiazepine cleared by the FDA?

Il Test(Tm) Benzodiazepine (K914815) received a 510(k) decision of Substantially Equivalent on January 27, 1992, 94 days after the submission was received.

What is the product code of K914815?

The FDA product code is JXM – Enzyme Immunoassay, Benzodiazepine, a Class II (moderate risk) device regulated under 21 CFR 862.3170.