510(k) K243341

Device
Genius AI Detection 2.0
Applicant
Hologic, Inc.
510(k) number
K243341
Product code
QDQ
Decision
Substantially Equivalent (SESE)
Decision date
2025-07-31
Date received
2024-10-25
Regulation
892.2090
Classification name
Radiological Computer Assisted Detection/Diagnosis Software For Lesions Suspicious For Cancer
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Julia Vaillancourt
Address
600 Technology Dr. Newark DE US 19702 19702

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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