FAQ 101
K-Number: K222012 · 2023-04-05
Device Summary
Frequently Asked Questions
What is the FAQ 101?
FAQ 101 is a medical device that received FDA 510(k) clearance on 2023-04-05. The listed applicant is Foreo, Inc.. The 510(k) number is K222012.
When did FAQ 101 receive FDA 510(k) clearance?
FAQ 101 received FDA 510(k) clearance on 2023-04-05, under 510(k) number K222012.
Who is the listed applicant for FAQ 101?
The FDA 510(k) record lists Foreo, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FAQ 101?
The FDA product code for FAQ 101 is PAY.
Other records listing Foreo, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: PAY)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.