FDA 510(k) Applications Submitted by OMRI KESLER
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K150035 | 01/09/2015 | V10 system | VIORA LTD. |
| K142093 | 08/01/2014 | V20 SYSTEM | VIORA LTD. |
| K152611 | 09/14/2015 | V20 system | VIORA LTD. |
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