Chemtrue BUP/TCA Single/Multi-Panel Drug Screen Dip Card/Cup/Cassette Tests

FDA 510(k) K142396 · Chemtron Biotech, Inc.

Substantially Equivalent

510(k) numberK142396

Submission

Device name
Chemtrue BUP/TCA Single/Multi-Panel Drug Screen Dip Card/Cup/Cassette Tests
Applicant
Chemtron Biotech, Inc.
San Diego, CA, US
Received
August 27, 2014
Decision date
October 9, 2014
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DJG – Enzyme Immunoassay, Opiates
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3650
Specialty
Clinical Toxicology

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More from Shanghai Accurature Diagnostics Co., Ltd.

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K232736Chemtrue® Drug Screen Fentanyl/Tramadol Cup Test, Chemtrue® Drug Screen…DJG · Traditional 12/20/2023SE
K153192Chemtrue Multi-Panel Drug Screen Dip Card/Cup Tests, Chemtrue Multi-Panel Drug Screen…DJG · Traditional 04/18/2016SE
K143599Chemtrue Drug Screen Cup Tests and Chemtrue Drug Screen Cup Tests with OPI 2000DJG · Traditional 04/17/2015SE
K142580Chemtrue Multi-Panel DOA DIP Card TestsDKZ · Special 12/01/2014SE
K131931Chemtrue(R) HCG Pregnancy Urine Midstream TestLCX · Traditional 07/26/2013SE
K123844Chemtrue HCG Pregnancy Urine Dipstick, HCG Pregnancy Urine Cassette Test, and HCG Combo…JHI · Traditional 05/30/2013SE
K123080Chemtrue Single/Multi-Panel Drug Screen Dip Card/ Cassette TestsJXM · Traditional 11/29/2012SE
K121339Chemtrue Single/Multi-Panel Drug Screen Dip Card/Cassette TestsDKZ · Traditional 05/17/2012SE
K111322Chemtrue Single/Multi-Panel Drug Screen Cassette/DipcardJXM · Traditional 09/14/2011SE
K102203Chemtrue Single / Multi Drug Screen Cassette / Dip Card TestsDKZ · Traditional 01/20/2011SE

Questions and answers

When was Chemtrue BUP/TCA Single/Multi-Panel Drug Screen Dip Card/Cup/Cassette Tests cleared by the FDA?

Chemtrue BUP/TCA Single/Multi-Panel Drug Screen Dip Card/Cup/Cassette Tests (K142396) received a 510(k) decision of Substantially Equivalent on October 9, 2014, 43 days after the submission was received.

What is the product code of K142396?

The FDA product code is DJG – Enzyme Immunoassay, Opiates, a Class II (moderate risk) device regulated under 21 CFR 862.3650.