FDA 510(k) Applications Submitted by MICOMED GMBH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K991862 | 06/01/1999 | MICOMED POSTERIOR DOUBLEROD SYSTEM (MPDS) | MICOMED GMBH |
| K982006 | 06/08/1998 | MICOMED - HALM ZIELKE INSTRUMENTATION | MICOMED GMBH |
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