European Concerted Action on Anticoagulation is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
European Concerted Action on Anticoagulation - FDA 510(k) Cleared Dev...
1
Total
1
Cleared
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Denied
European Concerted Action on Anticoagulation has 1 FDA 510(k) cleared medical devices. Based in Manchester, GB.
Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by European Concerted Action on Anticoagulation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - European Concerted Action on Anticoagulation
1 devices