One Step Urine Drug of Abuse Methamphetamine Test
FDA 510(k) K970265 · Drial Consultants, Inc.
510(k) numberK970265
Submission
- Device name
- One Step Urine Drug of Abuse Methamphetamine Test
- Applicant
- Drial Consultants, Inc.
Simi Valley, CA, US - Received
- January 23, 1997
- Decision date
- April 8, 1997
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DKZ – Enzyme Immunoassay, Amphetamine
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.3100
- Specialty
- Clinical Toxicology
Other 510(k)s with product code DKZ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K240670 | DRI Ecstasy Plus AssayDKZ · Special | Microgenics Corporation | 10/30/2024SE |
| K233019 | AllTest Multi-Drug Rapid Test Cup; AllTest Multi-Drug Rapid Test Panel; AllTest…DKZ · Traditional | Hangzhou AllTest Biotech Co., Ltd. | 12/13/2023SE |
| K231137 | Xenta Drug Screen Cup, Xenta Drug Screen DipcardDKZ · Traditional | Xenta Biomedical Science Co., Ltd. | 05/19/2023SE |
| K200363 | Quidel Triage® TOX Drug Screen, 94600DKZ · Special | Quidel Cardiovascular, Inc. | 03/11/2020SE |
| K191099 | Atlas Multi-Drugs Screening Test Cup, Atlas Multi-Drugs Screening Test PanelDKZ · Traditional | Atlas Medical | 10/03/2019SE |
| K182719 | Quidel Triage TOX Drug Screen, 94600; Quidel Triage® MeterProDKZ · Traditional | Quidel Cardiovascular, Inc. | 06/19/2019SE |
| K182738 | Single and Multi-Drug Rapid Test Panel With Adulteration (Urine), Single and Multi-Drug…DKZ · Traditional | Hangzhou AllTest Biotech Co., Ltd. | 03/27/2019SE |
| K180879 | BIO-VENTURE Rapid Multi-Drug Test Easy Cup for OTC Use, BIO-VENTURE Rapid Multi-Drug…DKZ · Traditional | Shanghai Venture Bio-Tech Co., Ltd. | 12/14/2018SE |
| K181945 | QuickScreen Pro Multi Drug Screening Test, Model 9395ZDKZ · Traditional | Phamatech, Inc. | 10/18/2018SE |
| K173303 | INSTANT-VIEW plus Multi-Drug of Abuse Urine Test - Simple Cup (OTC Use), INSTANT-VIEW…DKZ · Traditional | Alfa Scientific Designs, Inc. | 02/23/2018SE |
More from Alfa Scientific Designs, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K973269 | Quikstrip One Step Benzodiazepine TestJXM · Traditional | 02/25/1998SE |
| K973326 | Quikpac II One Step Benzodiazepine TestJXM · Traditional | 02/24/1998SE |
| K973047 | One Step Urine Drug of Abuse Barbiturate TestDIS · Traditional | 10/02/1997SE |
| K972059 | Quikpac II One Step Cocaine TestDIO · Traditional | 08/28/1997SE |
| K972571 | Quikstrip One Step Opiates TestDJG · Traditional | 08/20/1997SE |
| K972405 | Quikpac II One Step Opiate TestDJG · Traditional | 08/08/1997SE |
| K971926 | Quikstrip One Step Cocaine TestDIO · Traditional | 07/14/1997SE |
| K970395 | Quikstrip One Step MethamphetamineDKZ · Traditional | 06/26/1997SE |
| K971218 | Quikstrip One Step Amphetamine TestDKZ · Traditional | 05/30/1997SE |
| K971109 | Quikpac II One Step Amphetamine TestDKZ · Traditional | 05/14/1997SE |
Questions and answers
When was One Step Urine Drug of Abuse Methamphetamine Test cleared by the FDA?
One Step Urine Drug of Abuse Methamphetamine Test (K970265) received a 510(k) decision of Substantially Equivalent on April 8, 1997, 75 days after the submission was received.
What is the product code of K970265?
The FDA product code is DKZ – Enzyme Immunoassay, Amphetamine, a Class II (moderate risk) device regulated under 21 CFR 862.3100.