Fibertech Instruments, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Fibertech Instruments, Inc. has 2 FDA 510(k) cleared medical devices. Based in Baltimore, US.
Historical record: 2 cleared submissions from 1994 to 1995. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Fibertech Instruments, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Fibertech Instruments, Inc.
2 devices