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FDA 510(k)

Clicky Cross

K-Number: K210516 · 2022-05-16

ApplicantYomura Technologies, Inc.
Decision Date2022-05-16
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Clicky Cross is the device name listed in this FDA 510(k) record. The listed applicant is Yomura Technologies, Inc.. It received FDA 510(k) clearance on 2022-05-16 under 510(k) number K210516. The device is classified under product code FMG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Clicky Cross?

Clicky Cross is a medical device that received FDA 510(k) clearance on 2022-05-16. The listed applicant is Yomura Technologies, Inc.. The 510(k) number is K210516.

When did Clicky Cross receive FDA 510(k) clearance?

Clicky Cross received FDA 510(k) clearance on 2022-05-16, under 510(k) number K210516.

Who is the listed applicant for Clicky Cross?

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

What is the FDA product code for Clicky Cross?

The FDA product code for Clicky Cross is FMG.

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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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