JZD
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Snare, Ear
- 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 |
|---|---|---|
| FIBRINOGEN UPTAKE SYS -VARIOUS MODELS (K834168) | Canberra Industries, Inc. | 1983-12-29 |
| EAR SNARES (K822199) | Kelleher Corp. | 1982-08-25 |
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