FDA 510(k), K852069, MECTA ECT DEVICE MODELS SR & JR
FDA 510(k), K852069, MECTA ECT DEVICE MODELS SR & JR
Device Name: MECTA ECT DEVICE MODELS SR & JR
Manufacturer:
Device Classification Name: Electroconvulsive Therapy Device For Catatonia, Major Depressive Disorder, And Bipolar Disorder
Regulation Number: 882.5940
Classification Product Code: QGH
Date Received: 05/10/1985
Decision Date: 08/09/1985
Regulation Medical Specialty: Neurology
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