Cortium™
K-Number: K230614 · 2023-05-02
Device Summary
Frequently Asked Questions
What is the Cortium™?
Cortium™ is a medical device that received FDA 510(k) clearance on 2023-05-02. The listed applicant is Ulrich Medical USA. The 510(k) number is K230614.
When did Cortium™ receive FDA 510(k) clearance?
Cortium™ received FDA 510(k) clearance on 2023-05-02, under 510(k) number K230614.
Who is the listed applicant for Cortium™?
The FDA 510(k) record lists Ulrich Medical USA as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cortium™?
The FDA product code for Cortium™ is NKG.
Other records listing Ulrich Medical USA as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: NKG)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.