New Low Level Drug Mixture Control
FDA 510(k) K890030 · Rapid Diagnostic Laboratories, Inc.
510(k) numberK890030
Submission
- Device name
- New Low Level Drug Mixture Control
- Applicant
- Rapid Diagnostic Laboratories, Inc.
Port Washington, NY, US - Received
- January 4, 1989
- Decision date
- January 23, 1989
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- DIF – Drug Mixture Control Materials
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 862.3280
- Specialty
- Clinical Toxicology
Other 510(k)s with product code DIF
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K153474 | Detectabuse Liquid Control Urine, Detectabuse Stat-Skreen Liquid Control Urine…DIF · Traditional | Biochemical Diagnostics, Inc. | 02/23/2016SE |
| K132688 | Salivabuse Liquid Oral Fluid Control, Salivabuse Liquid Oral Fluid Control, Au/NzDIF · Traditional | Biochemical Diagnostics, Inc. | 12/16/2013SE |
| K132174 | Multichem WBTDIF · Abbreviated | Techno-Path Manufacturing , Ltd. | 09/20/2013SE |
| K121122 | Detectabuse Liquid Control, Detectabuse Stat-Skreen Liquid ControlDIF · Traditional | Biochemical Diagnostic, Inc. | 07/03/2012SE |
| K121143 | Liquichek Whole Blood Immunosuppressant Control Tilevel (1,2 and 3)DIF · Traditional | Bio-Rad Laboratories | 05/18/2012SE |
| K120504 | Liquichek Urine Toxicology Control, S10 & S10 Minipak, Liquichek Urine Toxicology…DIF · Traditional | Bio-Rad Laboratories, Inc. | 03/27/2012SE |
| K103656 | Thermo Scientific Mas R Doa TotalDIF · Traditional | Microgenics Corporation | 03/24/2011SE |
| K093577 | Liquichek Opiate ControlDIF · Traditional | Bio-Rad Laboratories | 03/12/2010SE |
| K080085 | Mas Tox ControlDIF · Traditional | Thermo Fisher Scientific | 04/30/2008SE |
| K080183 | Control Set Dat I, Contrl Set Dat II, Control Set Dat III, Control Set Amphetamine 1000…DIF · Abbreviated | Roche Diagnostics Corp. | 03/25/2008SE |
More from Roche Diagnostics Corp.
| 510(k) | Device | Decision |
|---|---|---|
| K903909 | Blind Controls for Drugs of Abuse TestingDIF · Traditional | 10/26/1990SE |
| K875216 | High Performance CalibratorsDKB · Traditional | 06/22/1988SE |
| K871694 | Hyperformance Controls (Hp-Controls)DIF · Traditional | 07/07/1987SE |
| K863117 | High Performance Cannabinoid ControlsLAS · Traditional | 09/25/1986SE |
| K850139 | Cobe Cop Filter Cardiopulmonary Prebypass FilterKRJ · Traditional | 04/10/1985SE |
Questions and answers
When was New Low Level Drug Mixture Control cleared by the FDA?
New Low Level Drug Mixture Control (K890030) received a 510(k) decision of Substantially Equivalent on January 23, 1989, 19 days after the submission was received.
What is the product code of K890030?
The FDA product code is DIF – Drug Mixture Control Materials, a Class I (low risk) device regulated under 21 CFR 862.3280.