Microline Screen for Opiates
FDA 510(k) K905491 · Drug Screening Systems, Inc.
510(k) numberK905491
Submission
- Device name
- Microline Screen for Opiates
- Applicant
- Drug Screening Systems, Inc.
Blackwood, NJ, US - Received
- December 7, 1990
- Decision date
- March 13, 1991
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- DJG – Enzyme Immunoassay, Opiates
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.3650
- Specialty
- Clinical Toxicology
Other 510(k)s with product code DJG
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K252684 | Labcorp Fentanyl Urine Visual TestDJG · Traditional | Medtox Diagnostics, Inc. | 01/29/2026SE |
| K250741 | Evidence MultiSTAT DOA Urine MultiPlexDJG · Traditional | Randox Laboratories Limited | 01/23/2026SE |
| K253082 | LZI Buprenorphine II Enzyme ImmunoassayDJG · Traditional | Lin-Zhi International, Inc. | 01/16/2026SE |
| K252520 | SEFRIA Hydrocodone Oral FluidDJG · Traditional | Immunalysis Corporation | 09/11/2025SE |
| K251972 | Healgen® AccuFluor Fentanyl Fluorescence Immunoassay (FIA)Test Kit - Qualitative…DJG · Traditional | Healgen Scientific,, LLC | 08/15/2025SE |
| K251634 | LZI Fentanyl III Enzyme ImmunoassayDJG · Special | Lin-Zhi International, Inc. | 06/18/2025SE |
| K240124 | BioSieve Fentanyl FIA Test Kit; BioSieve ToxiSmart FIA ReaderDJG · Traditional | Vivachek Biotech (Hangzhou) Co., Ltd. | 06/14/2024SE |
| K240698 | Dochek® Multi-Drug Urine Test Dipcard Rx; Dochek® Multi-Drug Urine Test DipcardDJG · Traditional | Guangzhou Decheng Biotechnology Co., Ltd. | 05/10/2024SE |
| K231904 | Rapid Fentanyl (FYL) Test Strip, Rapid Fentanyl (FYL) Test DipcardDJG · Traditional | Co-Innovation Biotech Co., Ltd. | 03/08/2024SE |
| K232228 | Multi-drug Urine Test Cup, Multi-drug Urine Test Dip Card, Accurature Multi-drug Urine…DJG · Traditional | Shanghai Accurature Diagnostics Co., Ltd. | 02/23/2024SE |
More from Shanghai Accurature Diagnostics Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K945829 | Microline Screen for BenzodiazepineJXM · Traditional | 01/25/1995SE |
| K935052 | Microline Screen for AmphetamineDKZ · Traditional | 09/16/1994SE |
| K933480 | Microline Screen for BarbituratesDIS · Traditional | 10/29/1993SE |
| K921651 | Microline Screen for PhencyclidineLCM · Traditional | 07/08/1992SE |
| K914915 | Microline Screen for CannabinoidLDJ · Traditional | 01/22/1992SE |
| K911652 | Mircoline Screen for CocaineDIO · Traditional | 05/15/1991SE |
| K910525 | Microline Screen for MethamphetamineDIT · Traditional | 04/05/1991SE |
Questions and answers
When was Microline Screen for Opiates cleared by the FDA?
Microline Screen for Opiates (K905491) received a 510(k) decision of Substantially Equivalent on March 13, 1991, 96 days after the submission was received.
What is the product code of K905491?
The FDA product code is DJG – Enzyme Immunoassay, Opiates, a Class II (moderate risk) device regulated under 21 CFR 862.3650.