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FDA 510(k), K863815, ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000
FDA 510(k), K863815, ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000
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510(K) Number: K863815
Device Name: ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000
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: 09/30/1986
Decision Date: 06/02/1987
Regulation Medical Specialty: Neurology
Device Name: ELECTROCONVULSIVE THERAPY DEVICE, MODEL MF-1000
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: 09/30/1986
Decision Date: 06/02/1987
Regulation Medical Specialty: Neurology
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