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FDA 510(k)

FAQ™ (102)

K-Number: K240616 · 2024-07-15

ApplicantForeo, Inc.
Decision Date2024-07-15
Product CodePAY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FAQ™ (102) is a medical device manufactured by Foreo, Inc.. It received FDA 510(k) clearance on 2024-07-15 under approval number K240616. The device is classified under product code PAY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FAQ™ (102)?

FAQ™ (102) is a medical device that received FDA 510(k) clearance on 2024-07-15. It is manufactured by Foreo, Inc.. The 510(k) number is K240616.

When was FAQ™ (102) approved by the FDA?

FAQ™ (102) received FDA 510(k) clearance on 2024-07-15, under approval number K240616.

What company makes FAQ™ (102)?

FAQ™ (102) is manufactured by Foreo, Inc..

What is the FDA product code for FAQ™ (102)?

The FDA product code for FAQ™ (102) is PAY.

Other Devices by Foreo, Inc.

K162450ESPADA Acne-Clearing Blue Light Pen K200803BEAR and BEAR mini K231977PEACH 2, PEACH 2 Duo, PEACH 2 go K222012FAQ 101 K242747FAQ™ (302) K241102Luna 4 plus

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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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