Acon Bzo One Step Benzodiazepines Test Strip; Acon Bzo One Step Benzodiazepines Test Device

FDA 510(k) K012300 · ACON Laboratories, Inc.

Substantially Equivalent

510(k) numberK012300

Submission

Device name
Acon Bzo One Step Benzodiazepines Test Strip; Acon Bzo One Step Benzodiazepines Test Device
Applicant
ACON Laboratories, Inc.
San Diego, CA, US
Received
July 20, 2001
Decision date
September 17, 2001
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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Questions and answers

When was Acon Bzo One Step Benzodiazepines Test Strip; Acon Bzo One Step Benzodiazepines Test Device cleared by the FDA?

Acon Bzo One Step Benzodiazepines Test Strip; Acon Bzo One Step Benzodiazepines Test Device (K012300) received a 510(k) decision of Substantially Equivalent on September 17, 2001, 59 days after the submission was received.

What is the product code of K012300?

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