FDA 510(k), K111717, ELECTRO-GEL
FDA 510(k), K111717, ELECTRO-GEL
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510(K) Number: K111717
Device Name: ELECTRO-GEL
Manufacturer:
Device Classification Name: Media, Electroconductive
Regulation Number: 882.1275
Classification Product Code: GYB
Date Received: 06/20/2011
Decision Date: 01/05/2012
Regulation Medical Specialty: Neurology
Device Name: ELECTRO-GEL
Manufacturer:
Device Classification Name: Media, Electroconductive
Regulation Number: 882.1275
Classification Product Code: GYB
Date Received: 06/20/2011
Decision Date: 01/05/2012
Regulation Medical Specialty: Neurology