Domino S.R.L.
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) | K071431 | GLOBUS GENESY 1100 STIMULATOR | IPF | 2007-09-21 | View |
| 510(k) | K061632 | GLOBUS PREMIUM MUSCLE STIMULATOR | NGX | 2007-04-30 | View |
No matching devices.
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