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FDA 510(k), K160237, Cefaly
FDA 510(k), K160237, Cefaly
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$149.00 USD
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$149.00 USD
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510(K) Number: K160237
Device Name: Cefaly
Manufacturer: CEFALY TECHNOLOGY
Device Classification Name: stimulator, nerve, electrical, transcutaneous, for migraine
Regulation Number: 882.5891
Classification Product Code: PCC
Date Received: 02/01/2016
Decision Date: 03/04/2016
Regulation Medical Specialty: Neurology
Device Name: Cefaly
Manufacturer: CEFALY TECHNOLOGY
Device Classification Name: stimulator, nerve, electrical, transcutaneous, for migraine
Regulation Number: 882.5891
Classification Product Code: PCC
Date Received: 02/01/2016
Decision Date: 03/04/2016
Regulation Medical Specialty: Neurology
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