Riemser Arzneimittel AG
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K113539 | REVOIS PRO IMPLANT STSYEM | DZE | 2013-05-03 | View |
| 510(k) | K113042 | REVOIS IMPLANT SYSTEM | DZE | 2013-03-08 | View |
| 510(k) | K120152 | CERASORB PLUS | NPM | 2012-08-13 | View |
No matching devices.
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