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FDA 510(k)

WITOUCH PRO

K-Number: K120398 · 2012-08-16

ApplicantHollywog, LLC
Decision Date2012-08-16
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

WITOUCH PRO is the device name listed in this FDA 510(k) record. The listed applicant is Hollywog, LLC. It received FDA 510(k) clearance on 2012-08-16 under 510(k) number K120398. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WITOUCH PRO?

WITOUCH PRO is a medical device that received FDA 510(k) clearance on 2012-08-16. The listed applicant is Hollywog, LLC. The 510(k) number is K120398.

When did WITOUCH PRO receive FDA 510(k) clearance?

WITOUCH PRO received FDA 510(k) clearance on 2012-08-16, under 510(k) number K120398.

Who is the listed applicant for WITOUCH PRO?

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?

The FDA product code for WITOUCH PRO is GZJ.

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Other records listing Hollywog, LLC as applicant

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.

K171599WiTouch Pro, WiTouch, NeubacK120500THE PAIN PILOT (A.K.A PAIN PILOT)

Related Devices (Code: GZJ)

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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