Radmedix, LLC - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Radmedix, LLC has 6 FDA 510(k) cleared medical devices. Based in Dayton, US.
Last cleared in 2023. Active since 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Radmedix, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kamm & Associates as regulatory consultant.
6 devices
Cleared
Oct 25, 2023
AcuityUDR
Radiology
112d
Cleared
Jul 12, 2023
AcuityDR 1013 G4, AcuityDR 1417 G4, AcuityDR 1717G4
Radiology
30d
Cleared
Apr 30, 2021
AcuityDRe
Radiology
32d
Cleared
May 06, 2020
Accuvue+
Radiology
15d
Cleared
Apr 13, 2020
AcuityPDR
Radiology
24d
Cleared
Jan 02, 2020
Acuity SDR Standard, Acuity SDR Plus, Acuity FDR Standard
Radiology
29d