FDA 510(k), K040183, BISX
FDA 510(k), K040183, BISX
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$149.00 USD
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510(K) Number: K040183
Device Name: BISX
Manufacturer:
Device Classification Name: Index-Generating Electroencephalograph Software
Regulation Number: 882.1400
Classification Product Code: OLW
Date Received: 01/27/2004
Decision Date: 02/25/2004
Regulation Medical Specialty: Neurology
Device Name: BISX
Manufacturer:
Device Classification Name: Index-Generating Electroencephalograph Software
Regulation Number: 882.1400
Classification Product Code: OLW
Date Received: 01/27/2004
Decision Date: 02/25/2004
Regulation Medical Specialty: Neurology