MRVClass II
Drink, Glucose Tolerance
21 CFR 862.1345 / Clinical Chemistry
MRV is the FDA product code for Drink, Glucose Tolerance, a class II device type, regulated under 21 CFR 862.1345. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and 3 recalls.
Classification record
- Product code
- MRV
- Device name
- Drink, Glucose Tolerance
- Regulation
- 21 CFR 862.1345
- Device class
- Class II
- Review panel
- Clinical Chemistry
- Submission type
- 510(k) exempt
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- No
- Ingested clearances
- 3
- Ingested recalls
- 3
Clearances, product code MRV
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 2003 | 1 |
| 2004 | 1 |
| 2012 | 1 |
Applicants with the most clearances
Product code MRV| Applicant | Clearances |
|---|---|
| Ever Scientific | 1 |
| Perk Scientific, Inc. | 1 |
| Vineland Syrup 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.
