Neitz Instruments Company, Ltd. - FDA 510(k) Cleared Devices

Neitz Instruments Company, Ltd. has 24 FDA 510(k) cleared ophthalmic devices. Based in Washington, US.

Historical record: 24 cleared submissions from 1994 to 1997.

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