FDA 510(k) Applications Submitted by Mespere LifeSciences Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K131085 | 04/18/2013 | CENTRAL VENOUS PRESSURE SYSTEM - MESPERE VENUS 1000 | MESPERE LIFESCIENCES INC. |
| K151776 | 07/01/2015 | Central Venous Pressure System | Mespere LifeSciences Inc. |
| K182242 | 08/20/2018 | VO200 û NeurOs Cerebral Oximetry System | Mespere LifeSciences Inc. |
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