Medical Device Manufacturer · JP , Settsu, Osaka

Kaneka Corp. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2011

Total

Cleared

Denied

Kaneka Corp. has 1 FDA 510(k) cleared medical devices. Based in Settsu, Osaka, JP.

Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: Ophthalmic.

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

Kaneka 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 - Kaneka Corp.

1 devices

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