WiTouch Pro, WiTouch, Neubac— 510(k) K171599
Substantially EquivalentHollywog, LLC
FDA 510(k) clearance K171599 for WiTouch Pro, WiTouch, Neubac, Substantially Equivalent on 2017-09-22. Applicant: Hollywog, LLC.
Clearance details
- Applicant
- Hollywog, LLC
- Product code
- Code NUH
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chattanooga, TN, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.