FAQ 101
K-Number: K222012 · 2023-04-05
ApplicantForeo, Inc.
Decision Date2023-04-05
Product CodePAY
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
FAQ 101 is a medical device manufactured by Foreo, Inc.. It received FDA 510(k) clearance on 2023-04-05 under approval number K222012. 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 101?
FAQ 101 is a medical device that received FDA 510(k) clearance on 2023-04-05. It is manufactured by Foreo, Inc.. The 510(k) number is K222012.
When was FAQ 101 approved by the FDA?
FAQ 101 received FDA 510(k) clearance on 2023-04-05, under approval number K222012.
What company makes FAQ 101?
FAQ 101 is manufactured by Foreo, Inc..
What is the FDA product code for FAQ 101?
The FDA product code for FAQ 101 is PAY.
Other Devices by Foreo, Inc.
Related Devices (Code: PAY)
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.