Medical Device Manufacturer · US , New York , NY

Konica Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1992

Total

Cleared

Denied

Konica Corp. has 5 FDA 510(k) cleared medical devices. Based in New York, US.

Historical record: 5 cleared submissions from 1992 to 1999. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Konica Corp.

5 devices

1-5 of 5