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/ Hollywog, LLC
Hollywog, LLC
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K171599
WiTouch Pro, WiTouch, Neubac
September 22, 2017
K150695
Modpod
August 13, 2015
K120500
THE PAIN PILOT (A.K.A PAIN PILOT)
August 20, 2012
K120398
WITOUCH PRO
August 16, 2012