Medical Device Manufacturer · US , Saint Louis , MO

E.C.I. USA Corporation - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2007

Total

Cleared

Denied

E.C.I. USA Corporation has 1 FDA 510(k) cleared medical devices. Based in Saint Louis, US.

Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by E.C.I. USA Corporation Filter by specialty or product code using the sidebar.

E.C.I. USA Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - E.C.I. USA Corporation

1 devices

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