Oridion Medical 1987 , Ltd. has 19 FDA 510(k) cleared anesthesiology devices. Based in Jerusalem, IL.

Historical record: 19 cleared submissions from 2001 to 2020.

Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.

FDA 510(k) Regulatory Record - Oridion Medical 1987 , Ltd.

19 devices
1-12 of 19
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