co_sos
1 records
fda
1 records
FDA Device Recall: AEM Disposable Electrodes, Device, Electrosurgical, Cutting and Coagulation and
2012-07-18
Class II — Encision is performing a field correction to their AEM Disposable Electrodes due to two consumer complaints reporting unanticipated alarms from the AEM monitor while using the device. This...
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SEC EDGAR
1 records
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