Benzodiazepines/Tricyclic Antidepressants by HPLC

FDA 510(k) K896744 · Bio-Rad

Substantially Equivalent

510(k) numberK896744

Submission

Device name
Benzodiazepines/Tricyclic Antidepressants by HPLC
Applicant
Bio-Rad
Hercules, CA, US
Received
November 30, 1989
Decision date
February 23, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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Questions and answers

When was Benzodiazepines/Tricyclic Antidepressants by HPLC cleared by the FDA?

Benzodiazepines/Tricyclic Antidepressants by HPLC (K896744) received a 510(k) decision of Substantially Equivalent on February 23, 1990, 85 days after the submission was received.

What is the product code of K896744?

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