FDA 510(k) Applications Submitted by Frank Gischer
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K210298 | 02/03/2021 | GR-14 Resin System | Pro3dure Medical GmbH |
| K211415 | 05/06/2021 | GR Splint Resin System | Pro3dure Medical GmbH |
| K212017 | 06/28/2021 | Thermeo System | Pro3dure Medical GmbH |
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