KCA
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Tonsillectome
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 874.4420
- Medical specialty
- Ear, Nose, Throat
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| Record | Firm | Date |
|---|---|---|
| MACKENZIE'S TONSILLECTOME (K822186) | Kelleher Corp. | 1982-08-25 |
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