FDA 510(k) Applications Submitted by GANSHORN Medizin Electronic GmbH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K160116 | 01/19/2016 | SpiroScout | GANSHORN MEDIZIN ELECTRONIC GMBH |
| K240706 | 03/14/2024 | PowerCube+ Series (PowerCube Body+); PowerCube+ Series (PowerCube Diffusion+); PowerCube+ Series (PowerCube Body+ / Diffusion+) | GANSHORN Medizin Electronic GmbH |
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