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FDA 510(k)

BriefCase-Triage

K-Number: K261317 · 2026-05-14

ApplicantAidoc Medical , Ltd.
Decision Date2026-05-14
Product CodeQAS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BriefCase-Triage is a medical device manufactured by Aidoc Medical , Ltd.. It received FDA 510(k) clearance on 2026-05-14 under approval number K261317. The device is classified under product code QAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BriefCase-Triage?

BriefCase-Triage is a medical device that received FDA 510(k) clearance on 2026-05-14. It is manufactured by Aidoc Medical , Ltd.. The 510(k) number is K261317.

When was BriefCase-Triage approved by the FDA?

BriefCase-Triage received FDA 510(k) clearance on 2026-05-14, under approval number K261317.

What company makes BriefCase-Triage?

BriefCase-Triage is manufactured by Aidoc Medical , Ltd..

What is the FDA product code for BriefCase-Triage?

The FDA product code for BriefCase-Triage is QAS.

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.

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