FDA 510(k) Applications Submitted by ROTEC MEDIZINTECHNIK GMBH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K992359 | 07/14/1999 | MRS-TITAN | ROTEC MEDIZINTECHNIK GMBH |
| K992403 | 07/19/1999 | MRP-TITAN | ROTEC MEDIZINTECHNIK GMBH |
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