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FDA 510(k), K131681, EYESEECAM VHIT
FDA 510(k), K131681, EYESEECAM VHIT
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510(K) Number: K131681
Device Name: EYESEECAM VHIT
Manufacturer: INTERACOUSTICS A/S
Device Classification Name: nystagmograph
Regulation Number: 882.1460
Classification Product Code: GWN
Date Received: 06/10/2013
Decision Date: 09/06/2013
Regulation Medical Specialty: Neurology
Device Name: EYESEECAM VHIT
Manufacturer: INTERACOUSTICS A/S
Device Classification Name: nystagmograph
Regulation Number: 882.1460
Classification Product Code: GWN
Date Received: 06/10/2013
Decision Date: 09/06/2013
Regulation Medical Specialty: Neurology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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