Mighty Wire Guide Wire
K-Number: K230418 · 2023-10-28
ApplicantMerit Medical Systems, Inc.
Decision Date2023-10-28
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Mighty Wire Guide Wire is a medical device manufactured by Merit Medical Systems, Inc.. It received FDA 510(k) clearance on 2023-10-28 under approval number K230418. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Mighty Wire Guide Wire?
Mighty Wire Guide Wire is a medical device that received FDA 510(k) clearance on 2023-10-28. It is manufactured by Merit Medical Systems, Inc.. The 510(k) number is K230418.
When was Mighty Wire Guide Wire approved by the FDA?
Mighty Wire Guide Wire received FDA 510(k) clearance on 2023-10-28, under approval number K230418.
What company makes Mighty Wire Guide Wire?
Mighty Wire Guide Wire is manufactured by Merit Medical Systems, Inc..
What is the FDA product code for Mighty Wire Guide Wire?
The FDA product code for Mighty Wire Guide Wire is DQX.
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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.