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FDA 510(k)

Nihon Kohden Vital Sign Telemeter

K-Number: K153707 · 2016-09-02

ApplicantNihon Kohden Corporation
Decision Date2016-09-02
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Nihon Kohden Vital Sign Telemeter is a medical device manufactured by Nihon Kohden Corporation. It received FDA 510(k) clearance on 2016-09-02 under approval number K153707. 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 Nihon Kohden Vital Sign Telemeter?

Nihon Kohden Vital Sign Telemeter is a medical device that received FDA 510(k) clearance on 2016-09-02. It is manufactured by Nihon Kohden Corporation. The 510(k) number is K153707.

When was Nihon Kohden Vital Sign Telemeter approved by the FDA?

Nihon Kohden Vital Sign Telemeter received FDA 510(k) clearance on 2016-09-02, under approval number K153707.

What company makes Nihon Kohden Vital Sign Telemeter?

Nihon Kohden Vital Sign Telemeter is manufactured by Nihon Kohden Corporation.

What is the FDA product code for Nihon Kohden Vital Sign Telemeter?

The FDA product code for Nihon Kohden Vital Sign Telemeter is MHX.

Other Devices by Nihon Kohden Corporation

K152305Nihon Kohden Afib Detection Program QP-039P K171765Nihon Kohden CO2 Monitor K171124Nihon Kohden Wireless Input Unit WEE-1200 K163644Nihon Kohden QP-160AK EEG Trend Program K163459Nihon Kohden Vital Sign Telemeter K161860TG-970P CO2 Sensor Kit

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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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