Mason-Keller Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mason-Keller Corp. - FDA 510(k) Cleared Devices
4
Total
0
Cleared
0
Denied
Mason-Keller Corp. has 0 FDA 510(k) cleared medical devices. Based in Roseland, US.
Historical record: 0 cleared submissions from 1994 to 1994. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Mason-Keller Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mason-Keller Corp.
4 devices