µCor Heart Failure and Arrhythmia Management System
K-Number: K172510 · 2018-05-11
ApplicantZoll Manufacturing Corporation
Decision Date2018-05-11
Product CodeMHX
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
µCor Heart Failure and Arrhythmia Management System is a medical device manufactured by Zoll Manufacturing Corporation. It received FDA 510(k) clearance on 2018-05-11 under approval number K172510. 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 µCor Heart Failure and Arrhythmia Management System?
µCor Heart Failure and Arrhythmia Management System is a medical device that received FDA 510(k) clearance on 2018-05-11. It is manufactured by Zoll Manufacturing Corporation. The 510(k) number is K172510.
When was µCor Heart Failure and Arrhythmia Management System approved by the FDA?
µCor Heart Failure and Arrhythmia Management System received FDA 510(k) clearance on 2018-05-11, under approval number K172510.
What company makes µCor Heart Failure and Arrhythmia Management System?
µCor Heart Failure and Arrhythmia Management System is manufactured by Zoll Manufacturing Corporation.
What is the FDA product code for µCor Heart Failure and Arrhythmia Management System?
The FDA product code for µCor Heart Failure and Arrhythmia Management System 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.