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FDA 510(k), K172271, Trackit T4 EEG Amplifier
FDA 510(k), K172271, Trackit T4 EEG Amplifier
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510(K) Number: K172271
Device Name: Trackit T4 EEG Amplifier
Manufacturer: Lifelines Ltd.
Device Classification Name: full-montage standard electroencephalograph
Regulation Number: 882.1400
Classification Product Code: GWQ
Date Received: 07/28/2017
Decision Date: 05/04/2018
Regulation Medical Specialty: Neurology
Device Name: Trackit T4 EEG Amplifier
Manufacturer: Lifelines Ltd.
Device Classification Name: full-montage standard electroencephalograph
Regulation Number: 882.1400
Classification Product Code: GWQ
Date Received: 07/28/2017
Decision Date: 05/04/2018
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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