FDA 510(k) Applications Submitted by SHERRY KIM
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K180011 | 01/02/2018 | Pulmonx Chartis Tablet Console | Pulmonx Corporation |
| K140185 | 01/24/2014 | OCELOT CATHETER, OCELOT PIXL CATHETER, LIGHTBOX CONSOLE | AVINGER, INC. |
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