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FDA 510(k)

Claritag Advanced

K-Number: K222356 · 2023-05-18

ApplicantDgi Technologies
Decision Date2023-05-18
Product CodeGEH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Claritag Advanced is a medical device manufactured by Dgi Technologies. It received FDA 510(k) clearance on 2023-05-18 under approval number K222356. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Claritag Advanced?

Claritag Advanced is a medical device that received FDA 510(k) clearance on 2023-05-18. It is manufactured by Dgi Technologies. The 510(k) number is K222356.

When was Claritag Advanced approved by the FDA?

Claritag Advanced received FDA 510(k) clearance on 2023-05-18, under approval number K222356.

What company makes Claritag Advanced?

Claritag Advanced is manufactured by Dgi Technologies.

What is the FDA product code for Claritag Advanced?

The FDA product code for Claritag Advanced is GEH.

Other Devices by Dgi Technologies

K190747Claritag

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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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