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FDA 510(k), K171414, qEEG-Pro
FDA 510(k), K171414, qEEG-Pro
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510(K) Number: K171414
Device Name: qEEG-Pro
Manufacturer: Brainmaster Technologies, Inc.
Device Classification Name: Normalizing Quantitative Electroencephalograph Software
Regulation Number: 882.1400
Classification Product Code: OLU
Date Received: 05/15/2017
Decision Date: 07/01/2018
Regulation Medical Specialty: Neurology
Device Name: qEEG-Pro
Manufacturer: Brainmaster Technologies, Inc.
Device Classification Name: Normalizing Quantitative Electroencephalograph Software
Regulation Number: 882.1400
Classification Product Code: OLU
Date Received: 05/15/2017
Decision Date: 07/01/2018
Regulation Medical Specialty: Neurology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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