Medical Device Manufacturer · US , Washington , DC

Koike Medical Co. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1997

Total

Cleared

Denied

Koike Medical Co. has 1 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Koike Medical Co. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Koike Medical Co.

1 devices

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