BriefCase-Quantification
K-Number: K231631 · 2023-11-28
ApplicantAidoc Medical , Ltd.
Decision Date2023-11-28
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
BriefCase-Quantification is a medical device manufactured by Aidoc Medical , Ltd.. It received FDA 510(k) clearance on 2023-11-28 under approval number K231631. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the BriefCase-Quantification?
BriefCase-Quantification is a medical device that received FDA 510(k) clearance on 2023-11-28. It is manufactured by Aidoc Medical , Ltd.. The 510(k) number is K231631.
When was BriefCase-Quantification approved by the FDA?
BriefCase-Quantification received FDA 510(k) clearance on 2023-11-28, under approval number K231631.
What company makes BriefCase-Quantification?
BriefCase-Quantification is manufactured by Aidoc Medical , Ltd..
What is the FDA product code for BriefCase-Quantification?
The FDA product code for BriefCase-Quantification is JAK.
Other Devices by Aidoc Medical , Ltd.
Related Devices (Code: JAK)
K162302Somatom Confidence ® RT ProSiemens Medical Solutions USA, Inc.
K163213Revolution CTGe Medical Systems, LLC
K161157Vitrea CT Dual Energy Image ViewVital Images, Inc.
K160723OnSight 3D Extremity SystemCarestream Health, Inc.
K161196SOMATOM DriveSiemens Medical Solutions USA, Inc.
K161748SUPRIA w/guideShot OptionHitachi Medical Systems America, Inc.
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.