FDA 510(k) Applications Submitted by HANS GUENTER OSIEK
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K052473 | 09/09/2005 | CX 250 C PLUS WITH GAMMAXP SOFTWARE, MODEL 0121 0000 | INTER MEDICAL MEDIZINTECHNIK GMBH |
| K230393 | 02/14/2023 | UniCam Evo Software | Inter Medical Medizintechnik GmbH |
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