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FDA 510(k), K122149, QBTES
FDA 510(k), K122149, QBTES
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510(K) Number: K122149
Device Name: QBTES
Manufacturer: HANS BOSTROM
Device Classification Name: Recorder, Attention Task Performance
Regulation Number: LQD
Classification Product Code: 07/19/2012
Date Received: 10/17/2012
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
Device Name: QBTES
Manufacturer: HANS BOSTROM
Device Classification Name: Recorder, Attention Task Performance
Regulation Number: LQD
Classification Product Code: 07/19/2012
Date Received: 10/17/2012
Decision Date: Substantially Equivalent (SESE)
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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