FDA 510(k)

Cary

K号: K251111 · 2025-05-07

决定日期2025-05-07

产品代码JCX

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决定实质等同

器械摘要

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.

常见问题

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.

相关器械（代码：JCX）

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