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FDA 510(k)

Eagle device

K-Number: K230722 · 2023-12-08

ApplicantBelkin Vision, Ltd.
Decision Date2023-12-08
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

Eagle device is a medical device manufactured by Belkin Vision, Ltd.. It received FDA 510(k) clearance on 2023-12-08 under approval number K230722. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Eagle device?

Eagle device is a medical device that received FDA 510(k) clearance on 2023-12-08. It is manufactured by Belkin Vision, Ltd.. The 510(k) number is K230722.

When was Eagle device approved by the FDA?

Eagle device received FDA 510(k) clearance on 2023-12-08, under approval number K230722.

What company makes Eagle device?

Eagle device is manufactured by Belkin Vision, Ltd..

What is the FDA product code for Eagle device?

The FDA product code for Eagle device is HQF.

Other Devices by Belkin Vision, Ltd.

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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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