BriefCase
K-Number: K221240 · 2022-05-17
ApplicantAidoc Medical , Ltd.
Decision Date2022-05-17
Product CodeQAS
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
BriefCase is a medical device manufactured by Aidoc Medical , Ltd.. It received FDA 510(k) clearance on 2022-05-17 under approval number K221240. 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?
BriefCase is a medical device that received FDA 510(k) clearance on 2022-05-17. It is manufactured by Aidoc Medical , Ltd.. The 510(k) number is K221240.
When was BriefCase approved by the FDA?
BriefCase received FDA 510(k) clearance on 2022-05-17, under approval number K221240.
What company makes BriefCase?
BriefCase is manufactured by Aidoc Medical , Ltd..
What is the FDA product code for BriefCase?
The FDA product code for BriefCase 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.