Industrielle Entwicklung Medizintechnik Und Vertri is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Industrielle Entwicklung Medizintechnik Und Vertri - FDA 510(k) Clear...
2
Total
2
Cleared
0
Denied
Industrielle Entwicklung Medizintechnik Und Vertri has 2 FDA 510(k) cleared medical devices. Based in Stamford, US.
Historical record: 2 cleared submissions from 1999 to 2000. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Industrielle Entwicklung Medizintechnik Und Vertri Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Industrielle Entwicklung Medizintechnik Und Vertri
2 devices