FDA Product Code PLZ: Ocular Pattern Recorder
A Diurnal Pattern Recorder System Is A Non-implantable, Prescription Device Incorporating A Telemetric Sensor Intended To Detect Changes In Ocular Dimension For Monitoring Diurnal Patterns Of Iop Fluctuation.
1
Total
0
Cleared
668d
Avg days
2016
Since
FDA 510(k) Cleared Ocular Pattern Recorder Devices (Product Code PLZ)
1 devices
No devices found for this product code.