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FDA 510(k)

Cary

K-Number: K251111 · 2025-05-07

ApplicantExcitus AS
Decision Date2025-05-07
Product CodeJCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Cary is a medical device manufactured by Excitus AS. It received FDA 510(k) clearance on 2025-05-07 under approval 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. It is manufactured by Excitus AS. The 510(k) number is K251111.

When was Cary approved by the FDA?

Cary received FDA 510(k) clearance on 2025-05-07, under approval number K251111.

What company makes Cary?

Cary is manufactured by Excitus AS.

What is the FDA product code for Cary?

The FDA product code for Cary is 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.

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