Product code MVH
- Device name
- Device, Detection, Sulfide
- Medical specialty
- Dental
- Device class
- 2
- Regulation number
- 872.1870
- Review panel
- DE
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- Y
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset
Related 510(k) Records
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| DEN980003 | DIAMOND PROBE/PERIO 2000 SYSTEM | Diamond General Development Corp. | 1998-07-17 |