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WITOUCH PRO

Page Type
Cleared 510(K)
510(k) Number
K120398
510(k) Type
Traditional
Applicant
HOLLYWOG, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2012
Days to Decision
190 days
Submission Type
Summary

WITOUCH PRO

Page Type
Cleared 510(K)
510(k) Number
K120398
510(k) Type
Traditional
Applicant
HOLLYWOG, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2012
Days to Decision
190 days
Submission Type
Summary