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FDA 510(k)

VitalWatch Software User Interface

K-Number: K170973 · 2017-06-02

ApplicantVitalconnect, Inc.
Decision Date2017-06-02
Product CodeDRG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VitalWatch Software User Interface is a medical device manufactured by Vitalconnect, Inc.. It received FDA 510(k) clearance on 2017-06-02 under approval number K170973. The device is classified under product code DRG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VitalWatch Software User Interface?

VitalWatch Software User Interface is a medical device that received FDA 510(k) clearance on 2017-06-02. It is manufactured by Vitalconnect, Inc.. The 510(k) number is K170973.

When was VitalWatch Software User Interface approved by the FDA?

VitalWatch Software User Interface received FDA 510(k) clearance on 2017-06-02, under approval number K170973.

What company makes VitalWatch Software User Interface?

VitalWatch Software User Interface is manufactured by Vitalconnect, Inc..

What is the FDA product code for VitalWatch Software User Interface?

The FDA product code for VitalWatch Software User Interface is DRG.

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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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