Dan Med, Inc.
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K013210 | TRUWAVE | GZJ | 2002-04-04 | View |
| 510(k) | K012885 | NEUROMOVE NM900 | IPF | 2001-11-08 | View |
| 510(k) | K010745 | EMS 3000 | IPF | 2001-06-27 | View |
| 510(k) | K991241 | IF8000 | IPF | 1999-11-02 | View |
| 510(k) | K972997 | AM800 AUTOMOVE EMG TRIGGERED ELECTRICAL MUSCLE STIMULATION | IPF | 1997-11-10 | View |
| 510(k) | K964738 | ELPHA 2000 CONTI | KPI | 1997-08-14 | View |
No matching devices.
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