FDA 510(k), K911144, MF-500, MODIFICATION
FDA 510(k), K911144, MF-500, MODIFICATION
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$149.00 USD
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510(K) Number: K911144
Device Name: MF-500, MODIFICATION
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: 02/25/1991
Decision Date: 10/18/1991
Regulation Medical Specialty: Neurology
Device Name: MF-500, MODIFICATION
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: 02/25/1991
Decision Date: 10/18/1991
Regulation Medical Specialty: Neurology