Task Force CORE
K-Number: K223332 · 2023-04-12
ApplicantCnsystems Medizintechnik GmbH
Decision Date2023-04-12
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Task Force CORE is a medical device manufactured by Cnsystems Medizintechnik GmbH. It received FDA 510(k) clearance on 2023-04-12 under approval number K223332. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by Cnsystems Medizintechnik GmbH. The 510(k) number is K223332.
When was Task Force CORE approved by the FDA?
Task Force CORE received FDA 510(k) clearance on 2023-04-12, under approval number K223332.
What company makes Task Force CORE?
Task Force CORE is manufactured by Cnsystems Medizintechnik GmbH.
What is the FDA product code for Task Force CORE?
The FDA product code for Task Force CORE is DXN.
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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.