Kb & Assoc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kb & Assoc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Kb & Assoc. has 1 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 1 cleared submissions from 1983 to 1983. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Kb & Assoc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kb & Assoc.
1 devices