Medical Device Manufacturer · SE , Stockholm

Ekeroth Quality AB - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1999

Recent clearances: DYNAWELL OR DYNAWELL

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Ekeroth Quality AB Radiology ✕

1 devices

1-1 of 1

Cleared Aug 13, 1999

DYNAWELL OR DYNAWELL

Radiology · 51d