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FDA 510(k), K141865, DANA
FDA 510(k), K141865, DANA
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510(K) Number: K141865
Device Name: DANA
Manufacturer: ANTHROTRONIX, INC
Device Classification Name: recorder, attention task performance
Regulation Number:
Classification Product Code: LQD
Date Received: 07/10/2014
Decision Date: 10/15/2014
Regulation Medical Specialty:
Device Name: DANA
Manufacturer: ANTHROTRONIX, INC
Device Classification Name: recorder, attention task performance
Regulation Number:
Classification Product Code: LQD
Date Received: 07/10/2014
Decision Date: 10/15/2014
Regulation Medical Specialty:
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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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