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FDA 510(k)

Overjet Charting Assist

K-Number: K233590 · 2024-02-23

ApplicantOverjet, Inc.
Decision Date2024-02-23
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Overjet Charting Assist is a medical device manufactured by Overjet, Inc.. It received FDA 510(k) clearance on 2024-02-23 under approval number K233590. 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 Overjet Charting Assist?

Overjet Charting Assist is a medical device that received FDA 510(k) clearance on 2024-02-23. It is manufactured by Overjet, Inc.. The 510(k) number is K233590.

When was Overjet Charting Assist approved by the FDA?

Overjet Charting Assist received FDA 510(k) clearance on 2024-02-23, under approval number K233590.

What company makes Overjet Charting Assist?

Overjet Charting Assist is manufactured by Overjet, Inc..

What is the FDA product code for Overjet Charting Assist?

The FDA product code for Overjet Charting Assist is QIH.

Other Devices by Overjet, Inc.

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Related Devices (Code: QIH)

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.