KBI
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Bougie, Eustachian
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 874.4175
- Medical specialty
- Ear, Nose, Throat
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| BOUGIE, FILIFORM, JACKSON (K770959) | V. Mueller O.V. Baxter Healthcare Corp. | 1977-06-14 |
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Every clearance here is in the API, with alerts when new ones post.