Hosmer Dorrance Corp.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K822632 | ELBOW PROSTHESIS | IRE | 1982-09-14 | View |
| 510(k) | K821704 | FRACTURE BRACING | IQI | 1982-06-24 | View |
| 510(k) | K801788 | HUMEROUS FRACTURE BRACE, ULNA FRACTURE | IQI | 1980-08-07 | View |
| 510(k) | K780890 | CAPP TERMINAL DEVICE | IQX | 1978-06-13 | View |
| 510(k) | K780892 | FRACTURE BRACING | ITQ | 1978-06-13 | View |
| 510(k) | K780891 | POST-OPERATIVE HIP ORTHOSIS | ITS | 1978-06-13 | View |
| 510(k) | K761314 | FLEXION-BRAKING KNEE-SHIN ASSEMBLY | ION | 1977-01-10 | View |
| 510(k) | K761313 | 4-BAR KNEE-SHIN SET-UP | ION | 1977-01-10 | View |
| 510(k) | K761312 | ORTHOTIC BRACING | IQI | 1977-01-10 | View |
No matching devices.
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