Task Force CORE
K-Number: K223332 · 2023-04-12
Device Summary
Frequently Asked Questions
What is the Task Force CORE?
Task Force CORE is a medical device that received FDA 510(k) clearance on 2023-04-12. The listed applicant is Cnsystems Medizintechnik GmbH. The 510(k) number is K223332.
When did Task Force CORE receive FDA 510(k) clearance?
Task Force CORE received FDA 510(k) clearance on 2023-04-12, under 510(k) number K223332.
Who is the listed applicant for Task Force CORE?
The FDA 510(k) record lists Cnsystems Medizintechnik GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Task Force CORE?
The FDA product code for Task Force CORE is DXN.
Other records listing Cnsystems Medizintechnik GmbH 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: DXN)
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.