Sunmed, LLC
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) | K233098 | MYOTouch Muscle Stimulator | IPF | 2024-08-02 | View |
| 510(k) | K121743 | EASYMED PERIPHERAL NERVE STIMULATOR-SUNSTIN | BXN | 2013-03-28 | View |
No matching devices.
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