Known Identifiers & Locations
FEI Numbers
3007389703
Owner Operator Numbers
N/A
Locations Covered
N/A
Registered Establishments (0)
No device registration and listing records found for this entity.
510(k) Premarket Notifications (0)
No 510(k) notifications found for this entity.
FDA Recall History (1)
| Recall # |
Product Description |
Initiation Date |
Status |
Action |
| Z-0031-2022 |
Nox T3s Recorder - Product Usage: intended for ambulatory recording of physiological signals during sleep.
Reason: Error in the device firmware results in the inaccurate detection of device position.
|
2021-09-07 |
Terminated
|
View Details
|
Profile Disclaimer
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