FDA 510(k) Applications Submitted by OLYMPUS CORPORATION OF THE AMERICAS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K133538 | 11/18/2013 | VISERA CYSTO-NEPHRO VIDEOSCOPE OLYMPUS CYF TYPE V2, VISERA CYSTO-NEPHRO VIDEOSCOPE OLYMPUS CYF TYPE VA2, VISERA CYSTO-NE | OLYMPUS CORPORATION OF THE AMERICAS |
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