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FDA 510(k), K171186, Cerebrotech CMS-5000
FDA 510(k), K171186, Cerebrotech CMS-5000
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510(K) Number: K171186
Device Name: Cerebrotech CMS-5000
Manufacturer: Cerebrotech Medical Systems
Device Classification Name: impedance plethysmograph, cranial
Regulation Number: 870.2770
Classification Product Code: QAF
Date Received: 04/24/2017
Decision Date: 12/08/2017
Regulation Medical Specialty: Cardiovascular
Device Name: Cerebrotech CMS-5000
Manufacturer: Cerebrotech Medical Systems
Device Classification Name: impedance plethysmograph, cranial
Regulation Number: 870.2770
Classification Product Code: QAF
Date Received: 04/24/2017
Decision Date: 12/08/2017
Regulation Medical Specialty: Cardiovascular
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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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