I.E.M. Industrielle Entwicklung and Medizintechnik - FDA 510(k) Clear...
1
Total
1
Cleared
0
Denied
I.E.M. Industrielle Entwicklung and Medizintechnik has 1 FDA 510(k) cleared medical devices. Based in Stolberg, DE.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by I.E.M. Industrielle Entwicklung and Medizintechnik Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by I.E.M. Industrielle Entwicklung and...
1 devices