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FDA 510(k)

CNS-2101 Central Monitor

K-Number: K223567 · 2023-07-31

ApplicantNihon Kohden Corporation
Decision Date2023-07-31
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CNS-2101 Central Monitor is a medical device manufactured by Nihon Kohden Corporation. It received FDA 510(k) clearance on 2023-07-31 under approval number K223567. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CNS-2101 Central Monitor?

CNS-2101 Central Monitor is a medical device that received FDA 510(k) clearance on 2023-07-31. It is manufactured by Nihon Kohden Corporation. The 510(k) number is K223567.

When was CNS-2101 Central Monitor approved by the FDA?

CNS-2101 Central Monitor received FDA 510(k) clearance on 2023-07-31, under approval number K223567.

What company makes CNS-2101 Central Monitor?

CNS-2101 Central Monitor is manufactured by Nihon Kohden Corporation.

What is the FDA product code for CNS-2101 Central Monitor?

The FDA product code for CNS-2101 Central Monitor is MSX.

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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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