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FDA 510(k)

Customize

K-Number: K213779 · 2022-03-16

Applicant3D-Side S.A.
Decision Date2022-03-16
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Customize is a medical device manufactured by 3D-Side S.A.. It received FDA 510(k) clearance on 2022-03-16 under approval number K213779. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Customize?

Customize is a medical device that received FDA 510(k) clearance on 2022-03-16. It is manufactured by 3D-Side S.A.. The 510(k) number is K213779.

When was Customize approved by the FDA?

Customize received FDA 510(k) clearance on 2022-03-16, under approval number K213779.

What company makes Customize?

Customize is manufactured by 3D-Side S.A..

What is the FDA product code for Customize?

The FDA product code for Customize is QIH.

Other Devices by 3D-Side S.A.

K2122373D-Cut K221432Customize

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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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