Medical Device Manufacturer · JP , Kyoto

Kdk Corp. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1998

Total

Cleared

Denied

Kdk Corp. has 1 FDA 510(k) cleared medical devices. Based in Kyoto, JP.

Historical record: 1 cleared submissions from 1998 to 1998. Primary specialty: Chemistry.

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

Kdk Corp. is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Kdk Corp.

1 devices

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