QJL
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Splint, Intranasal Septal, Cber Led
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 874.4780
- Medical specialty
- Ear, Nose, Throat
- FDA definition
- Splint, Intranasal Septal, CBER led
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| SinuBand (K160101) | Bioinspire Technologies, Incorporated | 2016-07-27 |
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Every clearance here is in the API, with alerts when new ones post.