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FDA 510(k)

Finapres Nova Noninvasive Hemodynamic Monitor

K-Number: K160967 · 2017-04-18

ApplicantFinapres Medical Systems B.V.
Decision Date2017-04-18
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Finapres Nova Noninvasive Hemodynamic Monitor is a medical device manufactured by Finapres Medical Systems B.V.. It received FDA 510(k) clearance on 2017-04-18 under approval number K160967. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Finapres Nova Noninvasive Hemodynamic Monitor?

Finapres Nova Noninvasive Hemodynamic Monitor is a medical device that received FDA 510(k) clearance on 2017-04-18. It is manufactured by Finapres Medical Systems B.V.. The 510(k) number is K160967.

When was Finapres Nova Noninvasive Hemodynamic Monitor approved by the FDA?

Finapres Nova Noninvasive Hemodynamic Monitor received FDA 510(k) clearance on 2017-04-18, under approval number K160967.

What company makes Finapres Nova Noninvasive Hemodynamic Monitor?

Finapres Nova Noninvasive Hemodynamic Monitor is manufactured by Finapres Medical Systems B.V..

What is the FDA product code for Finapres Nova Noninvasive Hemodynamic Monitor?

The FDA product code for Finapres Nova Noninvasive Hemodynamic Monitor is DXN.

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Other Devices by Finapres Medical Systems B.V.

K173916Finapres Nova Noninvasive Hemodynamic Monitor

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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