Immucor Gti Diagnostics, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Immucor Gti Diagnostics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Waukesha, US.
Historical record: 2 cleared submissions from 2020 to 2020. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Immucor Gti Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Immucor Gti Diagnostics, Inc.
2 devices