JYK
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Holder, Ear Speculum
- 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 |
|---|---|---|
| SHEA'S EAR SPECULUM HOLDER PORT MANNS (K822011) | Kelleher Corp. | 1982-08-12 |
Track JYK automatically
Every clearance here is in the API, with alerts when new ones post.