KAG
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Holder, Speculum, Ent
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.1800
- Medical specialty
- General, Plastic Surgery
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| DRABKIN REAGENT (K842931) | E K Ind., Inc. | 1984-09-21 |
| CPI PRINTER (K822857) | Cardiac Pacemakers, Inc. | 1983-01-08 |
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Every clearance here is in the API, with alerts when new ones post.