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FDA 510(k)

North-vision Multi-parameter Patient Monitor

K-Number: K173036 · 2018-12-21

Decision Date2018-12-21
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

North-vision Multi-parameter Patient Monitor is the device name listed in this FDA 510(k) record. The listed applicant is North-Vision Tech., Inc.. It received FDA 510(k) clearance on 2018-12-21 under 510(k) number K173036. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the North-vision Multi-parameter Patient Monitor?

North-vision Multi-parameter Patient Monitor is a medical device that received FDA 510(k) clearance on 2018-12-21. The listed applicant is North-Vision Tech., Inc.. The 510(k) number is K173036.

When did North-vision Multi-parameter Patient Monitor receive FDA 510(k) clearance?

North-vision Multi-parameter Patient Monitor received FDA 510(k) clearance on 2018-12-21, under 510(k) number K173036.

Who is the listed applicant for North-vision Multi-parameter Patient Monitor?

The FDA 510(k) record lists North-Vision Tech., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for North-vision Multi-parameter Patient Monitor?

The FDA product code for North-vision Multi-parameter Patient Monitor is MHX.

Related Devices (Code: MHX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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