Hollywog, LLC
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) | K171599 | WiTouch Pro, WiTouch, Neubac | NUH | 2017-09-22 | View |
| 510(k) | K120500 | THE PAIN PILOT (A.K.A PAIN PILOT) | NUH | 2012-08-20 | View |
| 510(k) | K120398 | WITOUCH PRO | GZJ | 2012-08-16 | View |
No matching devices.
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