FDA 510(k) Applications Submitted by ALEX MILLER
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K062130 | 07/26/2006 | MEISINGER BENEX, MODEL BE001 | HAGER & MEISINGER GMBH |
| K122807 | 08/30/2012 | DENTAL IMPLANT SYSTEM | HAGER & MEISINGER GMBH |
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