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FDA 510(k)

Masimo Stork

K-Number: K234021 · 2024-05-03

ApplicantMasimo Corporation
Decision Date2024-05-03
Product CodeQYU
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Masimo Stork is a medical device manufactured by Masimo Corporation. It received FDA 510(k) clearance on 2024-05-03 under approval number K234021. The device is classified under product code QYU. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Masimo Stork?

Masimo Stork is a medical device that received FDA 510(k) clearance on 2024-05-03. It is manufactured by Masimo Corporation. The 510(k) number is K234021.

When was Masimo Stork approved by the FDA?

Masimo Stork received FDA 510(k) clearance on 2024-05-03, under approval number K234021.

What company makes Masimo Stork?

Masimo Stork is manufactured by Masimo Corporation.

What is the FDA product code for Masimo Stork?

The FDA product code for Masimo Stork is QYU.

Other Devices by Masimo Corporation

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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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