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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 the device name listed in this FDA 510(k) record. The listed applicant is Hollywog, LLC. It received FDA 510(k) clearance on 2017-09-22 under 510(k) 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. The listed applicant is Hollywog, LLC. The 510(k) number is K171599.

When did WiTouch Pro, WiTouch, Neubac receive FDA 510(k) clearance?

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

Who is the listed applicant for WiTouch Pro, WiTouch, Neubac?

The FDA 510(k) record lists Hollywog, LLC as the applicant. This does not by itself establish the device manufacturer.

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

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

Related Devices (Code: NUH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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

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