Vital Signs
K-Number: K243687 · 2025-08-27
ApplicantOxehealth Limited
Decision Date2025-08-27
Product CodeQME
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Vital Signs is a medical device manufactured by Oxehealth Limited. It received FDA 510(k) clearance on 2025-08-27 under approval number K243687. The device is classified under product code QME. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Vital Signs?
Vital Signs is a medical device that received FDA 510(k) clearance on 2025-08-27. It is manufactured by Oxehealth Limited. The 510(k) number is K243687.
When was Vital Signs approved by the FDA?
Vital Signs received FDA 510(k) clearance on 2025-08-27, under approval number K243687.
What company makes Vital Signs?
Vital Signs is manufactured by Oxehealth Limited.
What is the FDA product code for Vital Signs?
The FDA product code for Vital Signs is QME.
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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.