FDA 510(k), K010460, LIFELINES TRACKIT
FDA 510(k), K010460, LIFELINES TRACKIT
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510(K) Number: K010460
Device Name: LIFELINES TRACKIT
Manufacturer:
Device Classification Name: Standard Polysomnograph With Electroencephalograph
Regulation Number: 882.1400
Classification Product Code: OLV
Date Received: 02/16/2001
Decision Date: 05/14/2001
Regulation Medical Specialty: Neurology
Device Name: LIFELINES TRACKIT
Manufacturer:
Device Classification Name: Standard Polysomnograph With Electroencephalograph
Regulation Number: 882.1400
Classification Product Code: OLV
Date Received: 02/16/2001
Decision Date: 05/14/2001
Regulation Medical Specialty: Neurology