BriefCase-Triage
K-Number: K232751 · 2023-10-30
ApplicantAidoc Medical , Ltd.
Decision Date2023-10-30
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 2023-10-30 under approval number K232751. 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 2023-10-30. It is manufactured by Aidoc Medical , Ltd.. The 510(k) number is K232751.
When was BriefCase-Triage approved by the FDA?
BriefCase-Triage received FDA 510(k) clearance on 2023-10-30, under approval number K232751.
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.
Other Devices by Aidoc Medical , Ltd.
Related Devices (Code: 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.