BriefCase-Triage
K-Number: K243548 · 2024-12-11
ApplicantAidoc Medical , Ltd.
Decision Date2024-12-11
Product CodeQFM
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
BriefCase-Triage is a medical device manufactured by Aidoc Medical , Ltd.. It received FDA 510(k) clearance on 2024-12-11 under approval number K243548. The device is classified under product code QFM. 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 2024-12-11. It is manufactured by Aidoc Medical , Ltd.. The 510(k) number is K243548.
When was BriefCase-Triage approved by the FDA?
BriefCase-Triage received FDA 510(k) clearance on 2024-12-11, under approval number K243548.
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 QFM.
Other Devices by Aidoc Medical , Ltd.
Related Devices (Code: QFM)
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.