Livesure Barbiturates Screen Test
FDA 510(k) K012133 · Pan Probe Biotech, Inc.
510(k) numberK012133
Submission
- Device name
- Livesure Barbiturates Screen Test
- Applicant
- Pan Probe Biotech, Inc.
San Diego, CA, US - Received
- July 9, 2001
- Decision date
- July 20, 2001
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
- Third-party review
- Yes
Device classification
- Product code
- DIS – Enzyme Immunoassay, Barbiturate
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.3150
- Specialty
- Clinical Toxicology
Other 510(k)s with product code DIS
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K161714 | Immunalysis Barbiturates Urine Enzyme Immunoassay, Immunalysis Multi-Drug CalibratorsDIS · Traditional | Immunalysis Corporation | 10/14/2016SE |
| K151211 | AssureTech Secobarbital Strip, AssureTech Oxycodone Strip, AssureTech…DIS · Traditional | Assure Tech. Co., Ltd. | 06/04/2015SE |
| K150791 | Healgen Secobarbital Test(Strip, Cassette, Cup, Dip Card), Healgen Burprenorphine Test…DIS · Traditional | Healgen Scientific,, LLC | 04/24/2015SE |
| K143535 | CR3 Keyless Split Sample Cup Secobarbital- MethadoneDIS · Traditional | Guangzhou Wondfo Biotech Co., Ltd. | 01/13/2015SE |
| K140665 | GenPrime Snap-Top Split Key CupDIS · Traditional | Genprime, Inc. | 12/08/2014SE |
| K140215 | One Step Single/Multi-Drug Test Cup/DipcardDIS · Traditional | Co-Innovation Biotech Co., Ltd. | 06/16/2014SE |
| K092268 | Randox Bariturates AssayDIS · Traditional | Randox Laboratories, Ltd. | 05/25/2011SE |
| K110515 | Ucp Drug Screening Test CupsDIS · Special | Ucp Biosciences, Inc. | 04/20/2011SE |
| K070098 | Quickscreen Barbiturate 300 Screening Test, Models 9019, 9018; Multi Drug Screening…DIS · Traditional | Phamatech, Inc. | 12/07/2007SE |
| K070009 | At Home Drug Test Models, 9308T and 9308XDIS · Traditional | Phamatech, Inc. | 12/07/2007SE |
More from Phamatech, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K020968 | Livesure HCG Urinary Pregnancy Test Strip and Test CardJHI · Traditional | 07/15/2002SE |
| K013796 | Livesure Methadone Screen TestsDJR · Traditional | 11/26/2001SE |
| K012131 | Livesure Benzodiazepines Screen TestsJXM · Traditional | 07/20/2001SE |
| K012107 | Livesure Phenecycline (PCP) Screen TestsLCM · Traditional | 07/20/2001SE |
| K011610 | Livesure Methamphetamine Screen TestsLAF · Traditional | 06/08/2001SE |
| K011609 | Livesure Amphetamine Screen TestDKZ · Traditional | 06/08/2001SE |
| K010967 | Livesure Cocaine Screen TestDIO · Traditional | 04/17/2001SE |
| K011011 | Livesure Morphine Screen TestDOE · Traditional | 04/13/2001SE |
| K010001 | Livesure THC Screen TestLDJ · Traditional | 02/05/2001SE |
Questions and answers
When was Livesure Barbiturates Screen Test cleared by the FDA?
Livesure Barbiturates Screen Test (K012133) received a 510(k) decision of Substantially Equivalent on July 20, 2001, 11 days after the submission was received.
What is the product code of K012133?
The FDA product code is DIS – Enzyme Immunoassay, Barbiturate, a Class II (moderate risk) device regulated under 21 CFR 862.3150.