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FDA 510(k), K173916, Finapres Nova Noninvasive Hemodynamic Monitor
FDA 510(k), K173916, Finapres Nova Noninvasive Hemodynamic Monitor
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510(K) Number: K173916
Device Name: Finapres Nova Noninvasive Hemodynamic Monitor
Manufacturer: Iris van Uitert
Device Classification Name: System, Measurement, Blood-Pressure, Non-Invasive
Regulation Number: DXN
Classification Product Code: 12/22/2017
Date Received: 11/06/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: Finapres Nova Noninvasive Hemodynamic Monitor
Manufacturer: Iris van Uitert
Device Classification Name: System, Measurement, Blood-Pressure, Non-Invasive
Regulation Number: DXN
Classification Product Code: 12/22/2017
Date Received: 11/06/2018
Decision Date: Substantially Equivalent (SESE)
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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