Central Monitoring System (MFM-CMS)
K-Number: K232694 · 2024-02-05
ApplicantEdan Instruments, Inc.
Decision Date2024-02-05
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Central Monitoring System (MFM-CMS) is a medical device manufactured by Edan Instruments, Inc.. It received FDA 510(k) clearance on 2024-02-05 under approval number K232694. The device is classified under product code MHX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Central Monitoring System (MFM-CMS)?
Central Monitoring System (MFM-CMS) is a medical device that received FDA 510(k) clearance on 2024-02-05. It is manufactured by Edan Instruments, Inc.. The 510(k) number is K232694.
When was Central Monitoring System (MFM-CMS) approved by the FDA?
Central Monitoring System (MFM-CMS) received FDA 510(k) clearance on 2024-02-05, under approval number K232694.
What company makes Central Monitoring System (MFM-CMS)?
Central Monitoring System (MFM-CMS) is manufactured by Edan Instruments, Inc..
What is the FDA product code for Central Monitoring System (MFM-CMS)?
The FDA product code for Central Monitoring System (MFM-CMS) is MHX.
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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.