Instant-View Multi-Drug of Abuse Urine Test (Cup, Panel Cassette)

FDA 510(k) K131645 · Alfa Scientific Designs, Inc.

Substantially Equivalent

510(k) numberK131645

Submission

Device name
Instant-View Multi-Drug of Abuse Urine Test (Cup, Panel Cassette)
Applicant
Alfa Scientific Designs, Inc.
Powat, CA, US
Received
June 5, 2013
Decision date
October 7, 2013
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DKZ – Enzyme Immunoassay, Amphetamine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3100
Specialty
Clinical Toxicology

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More from Alfa Scientific Designs, Inc.

510(k)DeviceDecision
K173303INSTANT-VIEW plus Multi-Drug of Abuse Urine Test - Simple Cup (OTC Use), INSTANT-VIEW…DKZ · Traditional 02/23/2018SE
K173212Instant-view-PLUS immunochemical Fecal Occult Blood TestKHE · Traditional 02/15/2018SE
K152122Instant-View Multi-Drug Urine Test Cup (Home Use), Instant-View Multi-Drug Urine Test…DKZ · Traditional 06/24/2016SE
K100051Instant-View Milti-Drug of Abuse Urine Test (Panel, Cup), Instant-Verdict Multi-Drug of…DJG · Abbreviated 07/06/2010SE
K070660Instant-View Fecal Occult Blood (Fob) Rapid TestKHE · Traditional 06/21/2007SE
K063545Multi-Drug of Abuse Urine Test,Urine Cup Test, Amphetamine Urine Test(Cassette…DJG · Abbreviated 05/07/2007SE
K060527Instant-View Bup/Nbup Urine Test. Instant-Verdict Bup/Nbup Urine Test…DJG · Abbreviated 07/25/2006SE
K042227Instant-View Troponin I TestMMI · Traditional 11/19/2004SE
K024360Instant-View H. Pylori One Step Rapid TestLYR · Traditional 06/10/2003SE
K022693Instant-View Tca Urine TestMLK · Abbreviated 12/09/2002SE

Questions and answers

When was Instant-View Multi-Drug of Abuse Urine Test (Cup, Panel Cassette) cleared by the FDA?

Instant-View Multi-Drug of Abuse Urine Test (Cup, Panel Cassette) (K131645) received a 510(k) decision of Substantially Equivalent on October 7, 2013, 124 days after the submission was received.

What is the product code of K131645?

The FDA product code is DKZ – Enzyme Immunoassay, Amphetamine, a Class II (moderate risk) device regulated under 21 CFR 862.3100.