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FDA 510(k), K860467, ELECTROSHOCK UNIT NEUROLOGY MODEL B-25
FDA 510(k), K860467, ELECTROSHOCK UNIT NEUROLOGY MODEL B-25
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510(K) Number: K860467
Device Name: ELECTROSHOCK UNIT NEUROLOGY MODEL B-25
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: 02/06/1986
Decision Date: 11/10/1986
Regulation Medical Specialty: Neurology
Device Name: ELECTROSHOCK UNIT NEUROLOGY MODEL B-25
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: 02/06/1986
Decision Date: 11/10/1986
Regulation Medical Specialty: Neurology
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