BriefCase-Triage
K-Number: K253265 · 2025-11-06
Device Summary
Frequently Asked Questions
What is the BriefCase-Triage?
BriefCase-Triage is a medical device that received FDA 510(k) clearance on 2025-11-06. The listed applicant is Aidoc Medical , Ltd.. The 510(k) number is K253265.
When did BriefCase-Triage receive FDA 510(k) clearance?
BriefCase-Triage received FDA 510(k) clearance on 2025-11-06, under 510(k) number K253265.
Who is the listed applicant for BriefCase-Triage?
The FDA 510(k) record lists Aidoc Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BriefCase-Triage?
The FDA product code for BriefCase-Triage is QAS.
Other records listing Aidoc Medical , Ltd. 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: QAS)
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.