Medical Device Manufacturer · JP , Mie-Ken

Konica Medical and Graphic Corporation - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2003
1
Total
1
Cleared
0
Denied

Konica Medical and Graphic Corporation has 1 FDA 510(k) cleared medical devices. Based in Mie-Ken, JP.

Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Konica Medical and Graphic Corporation Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Konica Medical and Graphic Corporation
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