Cary
K-Number: K251111 · 2025-05-07
ApplicantExcitus AS
Decision Date2025-05-07
Product CodeJCX
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Cary is the device name listed in this FDA 510(k) record. The listed applicant is Excitus AS. It received FDA 510(k) clearance on 2025-05-07 under 510(k) number K251111. The device is classified under product code JCX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Cary?
Cary is a medical device that received FDA 510(k) clearance on 2025-05-07. The listed applicant is Excitus AS. The 510(k) number is K251111.
When did Cary receive FDA 510(k) clearance?
Cary received FDA 510(k) clearance on 2025-05-07, under 510(k) number K251111.
Who is the listed applicant for Cary?
The FDA 510(k) record lists Excitus AS as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cary?
The FDA product code for Cary is JCX.
Related Devices (Code: JCX)
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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.