Matrix Electromedical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Matrix Electromedical, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Matrix Electromedical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Las Vegas, US.
Historical record: 2 cleared submissions from 1993 to 1994. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Matrix Electromedical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Matrix Electromedical, Inc.
2 devices