Compagnie Oris Industrie, S.A.
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) | K881323 | CURIETRON 192 LOW DOSE RATE | JAQ | 1989-01-17 | View |
| 510(k) | K860311 | ACTHK-PR RIA KIT | CKG | 1986-04-07 | View |
No matching devices.
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