Report Studio
K-Number: K261747 · 2026-08-25
Device Summary
Frequently Asked Questions
What is the Report Studio?
Report Studio is a medical device that received FDA 510(k) clearance on 2026-08-25. The listed applicant is Beacon Biosignals, Inc.. The 510(k) number is K261747.
When did Report Studio receive FDA 510(k) clearance?
Report Studio received FDA 510(k) clearance on 2026-08-25, under 510(k) number K261747.
Who is the listed applicant for Report Studio?
The FDA 510(k) record lists Beacon Biosignals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Report Studio?
The FDA product code for Report Studio is OLV.
Other records listing Beacon Biosignals, 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: OLV)
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.