FullFocus
K-Number: K241273 · 2025-01-09
Device Summary
Frequently Asked Questions
What is the FullFocus?
FullFocus is a medical device that received FDA 510(k) clearance on 2025-01-09. The listed applicant is Paige.Ai, Inc.. The 510(k) number is K241273.
When did FullFocus receive FDA 510(k) clearance?
FullFocus received FDA 510(k) clearance on 2025-01-09, under 510(k) number K241273.
Who is the listed applicant for FullFocus?
The FDA 510(k) record lists Paige.Ai, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FullFocus?
The FDA product code for FullFocus is QKQ.
Other records listing Paige.Ai, 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: QKQ)
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.