Konica Minolta Healthcare Americas, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Konica Minolta Healthcare Americas, Inc. has 5 FDA 510(k) cleared medical devices. Based in Garner, US.
Last cleared in 2022. Active since 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Konica Minolta Healthcare Americas, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MEDIcept, Inc. as regulatory consultant.
5 devices