Koalaty Products, Inc.
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) | K102014 | TENS STIMULATOR, MODELS 2800 AND 3000 | GZJ | 2010-08-31 | View |
| 510(k) | K080661 | MODELS TENS 7000, EMS 7500 AND TWIN STIM | IPF | 2008-03-24 | View |
| 510(k) | K072795 | MODELS EMS 5.0, EMS 5.1 | IPF | 2007-11-27 | View |
No matching devices.
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