Kendall-Ltp is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kendall-Ltp - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Kendall-Ltp has 1 FDA 510(k) cleared medical devices. Based in Chicopee, US.
Historical record: 1 cleared submissions from 1996 to 1996. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Kendall-Ltp Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kendall-Ltp
1 devices