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FDA 510(k)

WiTouch Pro, WiTouch, Neubac

K-Number: K171599 · 2017-09-22

ApplicantHollywog, LLC
Decision Date2017-09-22
Product CodeNUH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

WiTouch Pro, WiTouch, Neubac is a medical device manufactured by Hollywog, LLC. It received FDA 510(k) clearance on 2017-09-22 under approval number K171599. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WiTouch Pro, WiTouch, Neubac?

WiTouch Pro, WiTouch, Neubac is a medical device that received FDA 510(k) clearance on 2017-09-22. It is manufactured by Hollywog, LLC. The 510(k) number is K171599.

When was WiTouch Pro, WiTouch, Neubac approved by the FDA?

WiTouch Pro, WiTouch, Neubac received FDA 510(k) clearance on 2017-09-22, under approval number K171599.

What company makes WiTouch Pro, WiTouch, Neubac?

WiTouch Pro, WiTouch, Neubac is manufactured by Hollywog, LLC.

What is the FDA product code for WiTouch Pro, WiTouch, Neubac?

The FDA product code for WiTouch Pro, WiTouch, Neubac is NUH.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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