510(k) K243808

Device
Rayvolve PTX-PE
Applicant
AZmed
510(k) number
K243808
Product code
QFM
Decision
Substantially Equivalent (SESE)
Decision date
2025-03-21
Date received
2024-12-11
Regulation
892.2080
Classification name
Radiological Computer-Assisted Prioritization Software For Lesions
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Anthony Joseph
Address
10 Rue D'Uzès Paris FR 75002 75002

FDA Registration Numbers

Source Documents

510(k) summary PDF

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