Masimo Stork
K-Number: K223721 · 2023-12-15
ApplicantMasimo Corporation
Decision Date2023-12-15
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Masimo Stork is a medical device manufactured by Masimo Corporation. It received FDA 510(k) clearance on 2023-12-15 under approval number K223721. The device is classified under product code DQA. 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 2023-12-15. It is manufactured by Masimo Corporation. The 510(k) number is K223721.
When was Masimo Stork approved by the FDA?
Masimo Stork received FDA 510(k) clearance on 2023-12-15, under approval number K223721.
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 DQA.
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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.