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FDA 510(k), K925111, HOUSE INFRARED/VIDEO ELECTRONYSTAGMOGRAPH SYSTEM
FDA 510(k), K925111, HOUSE INFRARED/VIDEO ELECTRONYSTAGMOGRAPH SYSTEM
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$149.00 USD
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510(K) Number: K925111
Device Name: HOUSE INFRARED/VIDEO ELECTRONYSTAGMOGRAPH SYSTEM
Manufacturer: EYE DYNAMICS, INC.
Device Classification Name: nystagmograph
Regulation Number: 882.1460
Classification Product Code: GWN
Date Received: 10/09/1992
Decision Date: 03/23/1994
Regulation Medical Specialty: Neurology
Device Name: HOUSE INFRARED/VIDEO ELECTRONYSTAGMOGRAPH SYSTEM
Manufacturer: EYE DYNAMICS, INC.
Device Classification Name: nystagmograph
Regulation Number: 882.1460
Classification Product Code: GWN
Date Received: 10/09/1992
Decision Date: 03/23/1994
Regulation Medical Specialty: Neurology
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