Mespere Lifesciences, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K182242 | VO200 – NeurOs Cerebral Oximetry System | QEM | 2018-12-26 | View |
| 510(k) | K131085 | CENTRAL VENOUS PRESSURE SYSTEM - MESPERE VENUS 1000 | PFA | 2013-08-22 | View |
No matching devices.
Advertisement