FDA 510(k) Applications Submitted by Immucor GTI Diagnostics, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K201311 | 05/18/2020 | PF4 IgG assay | Immucor GTI Diagnostics, Inc. |
| K201570 | 06/11/2020 | PF4 Enhanced assay | Immucor GTI Diagnostics, Inc. |
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