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FDA 510(k)

FAQ™ (302)

K-Number: K242747 · 2024-12-11

ApplicantForeo, Inc.
Decision Date2024-12-11
Product CodeOAP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FAQ™ (302) is a medical device manufactured by Foreo, Inc.. It received FDA 510(k) clearance on 2024-12-11 under approval number K242747. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FAQ™ (302)?

FAQ™ (302) is a medical device that received FDA 510(k) clearance on 2024-12-11. It is manufactured by Foreo, Inc.. The 510(k) number is K242747.

When was FAQ™ (302) approved by the FDA?

FAQ™ (302) received FDA 510(k) clearance on 2024-12-11, under approval number K242747.

What company makes FAQ™ (302)?

FAQ™ (302) is manufactured by Foreo, Inc..

What is the FDA product code for FAQ™ (302)?

The FDA product code for FAQ™ (302) is OAP.

Other Devices by Foreo, Inc.

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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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