Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1801667394
Device Listing 1801667394
Listing Summary
#
Listing key
1801667394
Premarket submission
K171599
Device
WiTouch Pro, WiTouch, Neubac
Applicant
Hollywog, LLC
Product code
NUH
Decision date
2017-09-22
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
134867
3008585473
3008585473
HOLLYWOG, LLC
1
N
2026-01-01
100 Cherokee Boulevard Chattanooga TN US 37405