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FDA 510(k)

Maestro Microcatheter

K-Number: K172081 · 2017-08-04

ApplicantMerit Medical Systems, Inc.
Decision Date2017-08-04
Product CodeKRA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Maestro Microcatheter is a medical device manufactured by Merit Medical Systems, Inc.. It received FDA 510(k) clearance on 2017-08-04 under approval number K172081. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Maestro Microcatheter?

Maestro Microcatheter is a medical device that received FDA 510(k) clearance on 2017-08-04. It is manufactured by Merit Medical Systems, Inc.. The 510(k) number is K172081.

When was Maestro Microcatheter approved by the FDA?

Maestro Microcatheter received FDA 510(k) clearance on 2017-08-04, under approval number K172081.

What company makes Maestro Microcatheter?

Maestro Microcatheter is manufactured by Merit Medical Systems, Inc..

What is the FDA product code for Maestro Microcatheter?

The FDA product code for Maestro Microcatheter is KRA.

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Related Devices (Code: KRA)

K161962VAMP Venous/Arterial Blood Management Protection SystemEdwards Lifesciences, LLC K160884CXI Support CatheterCook Incorporated K161921SwiftNINJA MicrocatheterMerit Medical Systems, Inc. K161402Bullfrog Micro-Infusion DeviceMercator Medsystems, Inc. K161801CrossCath Support CatheterCook Incorporated K153501Bullfrog Micro-Infusion DeviceMercator Medsystems, Inc.

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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