KBG
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Trocar, Sinus
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 874.4420
- Medical specialty
- Ear, Nose, Throat
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| REPROCESSED TROCARS (K033591) | Clearmedical, Inc. | 2005-06-03 |
| REPROCESSED DISPOSABLE TROCARS (K013987) | Adven Medical | 2002-03-01 |
| CONTINENT STOMA SYSTEM & ACCESSORIES (K844186) | Chesebrough-Pond'S U.S.A. Co. | 1985-01-15 |
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Every clearance here is in the API, with alerts when new ones post.