FDA 510(k) Applications Submitted by Christine Kishi
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K190332 | 02/14/2019 | Aperio AT2 DX System | Leica Biosystems Imaging, Inc. |
| K141109 | 04/29/2014 | APERIO EPATHOLOGY EIHC IVD SYSTEM | LEICA BIOSYSTEMS IMAGING, INC. |
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