Medical Device Manufacturer · US , Chattanooga , TN

Hollywog, LLC - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2012
4
Total
4
Cleared
0
Denied

FDA 510(k) Regulatory Record - Hollywog, LLC Neurology ✕

3 devices
1-3 of 3
Cleared Sep 22, 2017
WiTouch Pro, WiTouch, Neubac
K171599 · NUH
Neurology · 113d
Cleared Aug 20, 2012
THE PAIN PILOT (A.K.A PAIN PILOT)
K120500 · NUH
Neurology · 181d
Cleared Aug 16, 2012
WITOUCH PRO
K120398 · GZJ
Neurology · 190d
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