FDA 510(k) Applications Submitted by Ecleris USA
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K100595 | 03/02/2010 | ECLERIS MICROSTAR COLPOSCOPE | Ecleris USA |
| K131323 | 05/08/2013 | ECLERIS SINUSCOPE | Ecleris USA |
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