Medical Device Manufacturer · SE , Uppsala S-754 50

Scanditronix Medical AB - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1997

Total

Cleared

Denied

Scanditronix Medical AB has 4 FDA 510(k) cleared medical devices. Based in Uppsala S-754 50, SE.

Historical record: 4 cleared submissions from 1997 to 2001. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Scanditronix Medical AB

4 devices

1-4 of 4