FDA 510(k) Applications Submitted by LIDCO LTD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K152935 | 10/05/2015 | LiDCOunity Monitor | LIDCO LTD |
| K163334 | 11/28/2016 | LiDCOunity v2 Hemodynamic Monitor | LiDCO Ltd |
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