Instant-View Barbiturate Urine Cassette Test

FDA 510(k) K003647 · Alfa Scientific Designs, Inc.

Substantially Equivalent

510(k) numberK003647

Submission

Device name
Instant-View Barbiturate Urine Cassette Test
Applicant
Alfa Scientific Designs, Inc.
Poway, CA, US
Received
November 27, 2000
Decision date
May 29, 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
DIS – Enzyme Immunoassay, Barbiturate
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3150
Specialty
Clinical Toxicology

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More from Phamatech, Inc.

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K152122Instant-View Multi-Drug Urine Test Cup (Home Use), Instant-View Multi-Drug Urine Test…DKZ · Traditional 06/24/2016SE
K131645Instant-View Multi-Drug of Abuse Urine Test (Cup, Panel Cassette)DKZ · Abbreviated 10/07/2013SE
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
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Questions and answers

When was Instant-View Barbiturate Urine Cassette Test cleared by the FDA?

Instant-View Barbiturate Urine Cassette Test (K003647) received a 510(k) decision of Substantially Equivalent on May 29, 2001, 183 days after the submission was received.

What is the product code of K003647?

The FDA product code is DIS – Enzyme Immunoassay, Barbiturate, a Class II (moderate risk) device regulated under 21 CFR 862.3150.