FDA 510(k) Applications Submitted by Thomas Kuehl
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K130269 | 02/04/2013 | ECAT SCINTRON PET | MIE GMBH |
| K201807 | 07/01/2020 | ANCORIS | MiEGmbH |
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