FDA 510(k)

MICRUS COURIER ENZO MICROCATHETER 0.0190

K-Number: K072526 · 2007-10-05

ApplicantMicrus Endovascular Corporation

Decision Date2007-10-05

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MICRUS COURIER ENZO MICROCATHETER 0.0190 is the device name listed in this FDA 510(k) record. The listed applicant is Micrus Endovascular Corporation. It received FDA 510(k) clearance on 2007-10-05 under 510(k) number K072526. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRUS COURIER ENZO MICROCATHETER 0.0190?

MICRUS COURIER ENZO MICROCATHETER 0.0190 is a medical device that received FDA 510(k) clearance on 2007-10-05. The listed applicant is Micrus Endovascular Corporation. The 510(k) number is K072526.

When did MICRUS COURIER ENZO MICROCATHETER 0.0190 receive FDA 510(k) clearance?

MICRUS COURIER ENZO MICROCATHETER 0.0190 received FDA 510(k) clearance on 2007-10-05, under 510(k) number K072526.

Who is the listed applicant for MICRUS COURIER ENZO MICROCATHETER 0.0190?

The FDA 510(k) record lists Micrus Endovascular Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRUS COURIER ENZO MICROCATHETER 0.0190?

The FDA product code for MICRUS COURIER ENZO MICROCATHETER 0.0190 is DQO.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.