FDA 510(k), K223269, Spencer Probe Depth Electrodes
FDA 510(k), K223269, Spencer Probe Depth Electrodes
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510(K) Number: K223269
Device Name: Spencer Probe Depth Electrodes
Manufacturer: Brendan McCrea
Device Classification Name: Electrode, Depth
Regulation Number: GZL
Classification Product Code: 10/24/2022
Date Received: 05/18/2023
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
Device Name: Spencer Probe Depth Electrodes
Manufacturer: Brendan McCrea
Device Classification Name: Electrode, Depth
Regulation Number: GZL
Classification Product Code: 10/24/2022
Date Received: 05/18/2023
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
- 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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