Immucor Gti Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Immucor Gti Diagnostics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PF4 Enhanced assay, PF4 IgG assay
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) Regulatory Record - Immucor Gti Diagnostics, Inc.
2 devices