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FDA 510(k)

Masimo Root Monitoring System and Accessories

K-Number: K171121 · 2017-11-17

Decision Date2017-11-17
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Masimo Root Monitoring System and Accessories is a medical device manufactured by Masimo Corporation. It received FDA 510(k) clearance on 2017-11-17 under approval number K171121. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Masimo Root Monitoring System and Accessories?

Masimo Root Monitoring System and Accessories is a medical device that received FDA 510(k) clearance on 2017-11-17. It is manufactured by Masimo Corporation. The 510(k) number is K171121.

When was Masimo Root Monitoring System and Accessories approved by the FDA?

Masimo Root Monitoring System and Accessories received FDA 510(k) clearance on 2017-11-17, under approval number K171121.

What company makes Masimo Root Monitoring System and Accessories?

Masimo Root Monitoring System and Accessories is manufactured by Masimo Corporation.

What is the FDA product code for Masimo Root Monitoring System and Accessories?

The FDA product code for Masimo Root Monitoring System and Accessories is MWI.

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Official Source

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