Diagnostic devices · 21 CFR 872 Subpart B
Sulfide Detection Device
FDA device type “Device, Detection, Sulfide”.
- Companies listing it
- 00 makers
- Brands and models
- 0
- 510(k) clearances
- 10 in five years
- FDA name
- Device, Detection, Sulfide
510(k) clearances per year, 1976–2026
510(k) clearances
| Decided | 510(k) | Device | Applicant |
|---|---|---|---|
| 17 Jul 1998 | DEN980003 | DIAMOND PROBE/PERIO 2000 SYSTEM | Diamond General Development Corp. |
Official records: FDA product classification for MVH · 21 CFR 872.1870.
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026