Mighty Wire Guide Wire
K-Number: K230418 · 2023-10-28
Device Summary
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. The listed applicant is Merit Medical Systems, Inc.. The 510(k) number is K230418.
When did Mighty Wire Guide Wire receive FDA 510(k) clearance?
Mighty Wire Guide Wire received FDA 510(k) clearance on 2023-10-28, under 510(k) number K230418.
Who is the listed applicant for Mighty Wire Guide Wire?
The FDA 510(k) record lists Merit Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Mighty Wire Guide Wire?
The FDA product code for Mighty Wire Guide Wire is DQX.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Merit Medical Systems, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: DQX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.