Medical Device Manufacturer · US , Tokyo 100-91 Japan

Kamiya Tsusan Kaisha, Ltd. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1983

Total

Cleared

Denied

Kamiya Tsusan Kaisha, Ltd. has 4 FDA 510(k) cleared medical devices. Based in Tokyo 100-91 Japan, US.

Historical record: 4 cleared submissions from 1983 to 1986. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Kamiya Tsusan Kaisha, Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Kamiya Tsusan Kaisha, Ltd.

4 devices

1-4 of 4