Surgitek - FDA 510(k) Cleared Devices

Surgitek has 28 FDA 510(k) cleared gastroenterology & urology devices. Based in Mchenry, US.

Historical record: 28 cleared submissions from 1983 to 1995.

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