MVH
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Device, Detection, Sulfide
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 872.1870
- Medical specialty
- Dental
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| DIAMOND PROBE/PERIO 2000 SYSTEM (DEN980003) | Diamond General Development Corp. | 1998-07-17 |
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