MVOUnclassified
Kit, Test, Multiple, Drugs Of Abuse, Over The Counter
Unknown
MVO is the FDA product code for Kit, Test, Multiple, Drugs Of Abuse, Over The Counter. As of , FDA records hold 18 510(k) clearances under this code, the most recent dated , and one recall.
Classification record
- Product code
- MVO
- Device name
- Kit, Test, Multiple, Drugs Of Abuse, Over The Counter
- Device class
- Unclassified
- Review panel
- Unknown
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- No
- Ingested clearances
- 18
- Ingested recalls
- 1
Clearances, product code MVO
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1998 | 1 |
| 1999 | 5 |
| 2001 | 8 |
| 2002 | 2 |
| 2003 | 1 |
| 2004 | 1 |
Applicants with the most clearances
Product code MVO| Applicant | Clearances |
|---|---|
| Phamatech Inc. | 14 |
| Accu-Stat Diagnostics, Inc. | 1 |
| Advantage Diagnostics Corp. | 1 |
| Princeton BioMeditech Corp. | 1 |
| Texas Immunology, Inc. | 1 |
Companies listing this code with FDA
Companies whose registered establishments list this codeFIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
