FDA 510(k) Applications Submitted by ERIKA MARTIN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K062558 | 08/30/2006 | MESOSFOL SURGICAL FILM | BIOMET MANUFACTURING CORP. |
| K173319 | 10/20/2017 | KaVo NOMAD Pro 2 Handheld X-ray System | Aribex |
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