Shannon Group
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K820156 | THEIR ELECTRO SURGICAL COUTERY PENCIL | GEI | 1982-02-18 | View |
| 510(k) | K811205 | MOLDED POLYSULFONE TRIAL PROSTHESIS | HWT | 1981-05-21 | View |
No matching devices.
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