510(k) K232096

Device
Transpara Density 1.0.0
Applicant
Screenpoint Medical B.V.
510(k) number
K232096
Product code
QIH
Decision
Substantially Equivalent (SESE)
Decision date
2023-12-11
Date received
2023-07-13
Regulation
892.2050
Classification name
Automated Radiological Image Processing Software
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Robin Barwegen
Address
Mercator Ii, 7th Floor Toernooiveld 300 Nijmegen NL 6525 EC 6525 EC

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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