Eris Medical Technology
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) | K882295 | FILLING VOLUME OPTION | LJH | 1988-09-13 | View |
| 510(k) | K881878 | CATHETER WITHDRAWAL UNIT | KNY | 1988-07-28 | View |
| 510(k) | K850169 | ERIS URO-DIAGNOSTIC SYSTEM | FFG | 1985-04-22 | View |
No matching devices.
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