FDA 510(k) Applications Submitted by Burkhard Jakob
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K180443 | 02/20/2018 | Tumark Vision | SOMATEX Medical Technologies GmbH |
| K182082 | 08/02/2018 | Tumark for Eviva, Tumark for Brevera | Somatex Medical Technologies GmbH |
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