Clinical Micro Sensors
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- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Esensor Respiratory Viral Panel Ref K113731
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Esensor Cystic Fibrosis Carrier Detection Test, Esensor 4800 Dna Detection System, Model 4800 Ref K051435
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Clinical Micro Sensors have in the registry?
The registry currently lists 3 devices for Clinical Micro Sensors. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clinical Micro Sensors's devices?
Among its 3 most recently registered devices, Clinical Micro Sensors has devices listed in FDA 510(k) (3 devices).
What risk classes do Clinical Micro Sensors's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Clinical Micro Sensors's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clinical Micro Sensors in the registry?
The most recently registered devices listed for Clinical Micro Sensors include ESENSOR RESPIRATORY VIRAL PANEL, ESENSOR CYSTIC FIBROSIS CARRIER DETECTION SYSTEM, MODEL ESENSOR 4800 and ESENSOR CYSTIC FIBROSIS CARRIER DETECTION TEST, ESENSOR 4800 DNA DETECTION SYSTEM, MODEL 4800.