Valleylab,A Division of Tyco Healthcare Group LP is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Valleylab,A Division of Tyco Healthcare Group LP - FDA 510(k) Cleared...
2
Total
2
Cleared
0
Denied
Valleylab,A Division of Tyco Healthcare Group LP has 2 FDA 510(k) cleared medical devices. Based in Boulder, US.
Historical record: 2 cleared submissions from 2007 to 2007. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Valleylab,A Division of Tyco Healthcare Group LP Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Valleylab,A Division of Tyco Healthcare Group LP
2 devices