Microdyne, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Microdyne, Inc. has 1 FDA 510(k) cleared medical devices. Based in Valley Center, US.
Historical record: 1 cleared submissions from 1993 to 1993. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Microdyne, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Microdyne, Inc.
1 devices