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FDA 510(k)

Merit Pursue Microcatheter

K-Number: K173548 · 2018-03-30

ApplicantMerit Medical Systems, Inc.
Decision Date2018-03-30
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Merit Pursue Microcatheter is the device name listed in this FDA 510(k) record. The listed applicant is Merit Medical Systems, Inc.. It received FDA 510(k) clearance on 2018-03-30 under 510(k) number K173548. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Merit Pursue Microcatheter?

Merit Pursue Microcatheter is a medical device that received FDA 510(k) clearance on 2018-03-30. The listed applicant is Merit Medical Systems, Inc.. The 510(k) number is K173548.

When did Merit Pursue Microcatheter receive FDA 510(k) clearance?

Merit Pursue Microcatheter received FDA 510(k) clearance on 2018-03-30, under 510(k) number K173548.

Who is the listed applicant for Merit Pursue Microcatheter?

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 Merit Pursue Microcatheter?

The FDA product code for Merit Pursue Microcatheter is DQY.

Related Clinical Trials

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Related Devices (Code: DQY)

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.

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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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