Compex Technologies, Inc.
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) | K061516 | STAODYN MAX PRESET, MODEL 4470 | GZJ | 2007-02-06 | View |
| 510(k) | K050046 | REHABILICARE IF 3 WAVE INTERFERENTIAL STIMULATOR SYSTEM, MODEL 7110S | IPF | 2005-04-13 | View |
No matching devices.
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