Diagnostic devices · 21 CFR 872 Subpart B
Lead-Lined Radiographic Cone
FDA device type “Cone, Radiographic, Lead-Lined”.
- Companies listing it
- 00 makers
- Brands and models
- 0
- 510(k) clearances
- 20 in five years
- FDA name
- Cone, Radiographic, Lead-Lined
510(k) clearances per year, 1976–2026
510(k) clearances
| Decided | 510(k) | Device | Applicant |
|---|---|---|---|
| 16 Mar 1984 | K840275 | CEHPALOMETRIC HEAD POSITIONER | Gary E. Hall, Dds |
| 28 Sep 1977 | K771748 | INTRA ORAL X-RAY CONES | General Electric Co. |
Official records: FDA product classification for EAH · 21 CFR 872.1850.
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026