FDA 510(k) Applications Submitted by KURTIS MONTEGNA
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K120170 | 01/19/2012 | PROCARE PLUS VITRECTOMY SYSTEM | VISIONCARE DEVICES, INC. |
| K131790 | 06/18/2013 | A9800 ANESTHESIA WORKSTATION | ORICARE, INC. |
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