Cedia Dau Benzodiazepine Assay(Modification)

FDA 510(k) K954626 · Microgenics Corp.

Substantially Equivalent

510(k) numberK954626

Submission

Device name
Cedia Dau Benzodiazepine Assay(Modification)
Applicant
Microgenics Corp.
Concord, CA, US
Received
October 3, 1995
Decision date
November 27, 1995
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

Other 510(k)s with product code JXM

510(k)DeviceApplicantDecision
K243498Alinity c Benzodiazepines Reagent KitJXM · Special Microgenics Corporation12/11/2024SE
K221765ONLINE DAT Benzodiazepines IIJXM · Traditional Roche Diagnostics12/23/2022SE
K190968CEDIA Benzodiazepine AssayJXM · Traditional Microgenics Corporation12/09/2019SE
K173963DRI Benzodiazepine AssayJXM · Traditional Microgenics Corporation02/21/2018SE
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
K151642Heagen Multi-Drug Urine Test Cup, Healgen Multi-Drug Urine Test Dip CardJXM · Special Healgen Scientific,, LLC08/13/2015SE
K150356Healgen Multi-Drug Urine Test Cup, Healgen Multi-Drug Urine Test Dip CardJXM · Special Healgen Scientific,, LLC05/13/2015SE

More from Healgen Scientific,, LLC

510(k)DeviceDecision
K243498Alinity c Benzodiazepines Reagent KitJXM · Special 12/11/2024SE
K240670DRI Ecstasy Plus AssayDKZ · Special 10/30/2024SE
K231020Alinity c Tricyclic Antidepressants Reagent KitLFH · Traditional 11/17/2023SE
K231007CEDIA Heroin Metabolite (6-AM) AssayDJG · Traditional 09/27/2023SE
K213875DRI TM Tricyclics Serum Tox AssayLFH · Traditional 12/21/2022SE
K211973DRI Cocaine Metabolite AssayDIO · Traditional 09/24/2021SE
K192943CEDIA Heroin Metabolite (6-AM) assayDJG · Traditional 12/16/2019SE
K190968CEDIA Benzodiazepine AssayJXM · Traditional 12/09/2019SE
K181499DRI Cocaine Metabolite AssayDIO · Traditional 07/06/2018SE
K173963DRI Benzodiazepine AssayJXM · Traditional 02/21/2018SE

Questions and answers

When was Cedia Dau Benzodiazepine Assay(Modification) cleared by the FDA?

Cedia Dau Benzodiazepine Assay(Modification) (K954626) received a 510(k) decision of Substantially Equivalent on November 27, 1995, 55 days after the submission was received.

What is the product code of K954626?

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