WITOUCH PRO— 510(k) K120398

Substantially Equivalent

Hollywog, LLC

FDA 510(k) clearance K120398 for WITOUCH PRO, Substantially Equivalent on 2012-08-16. Applicant: Hollywog, LLC.

Clearance details

Applicant: Hollywog, LLC
Product code: Code GZJ
Advisory panel: Neurology
Date received: 2012-02-08
Decision date: 2012-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chattanooga, TN, US

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