Medical Device Manufacturer · US , Newburyport , MA

Scanditronix, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1984

Total

Cleared

Denied

Scanditronix, Inc. has 7 FDA 510(k) cleared medical devices. Based in Newburyport, US.

Historical record: 7 cleared submissions from 1984 to 1994. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Scanditronix, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Scanditronix, Inc.

7 devices

1-7 of 7