FDA 510(k)

MICRUS MICROCATHETER, COURIER FLEX, MODEL MSF 170000-00

K-Number: K083922 · 2009-05-06

ApplicantMicrus Endovascular Corporation

Decision Date2009-05-06

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MICRUS MICROCATHETER, COURIER FLEX, MODEL MSF 170000-00 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 2009-05-06 under 510(k) number K083922. 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 MICROCATHETER, COURIER FLEX, MODEL MSF 170000-00?

MICRUS MICROCATHETER, COURIER FLEX, MODEL MSF 170000-00 is a medical device that received FDA 510(k) clearance on 2009-05-06. The listed applicant is Micrus Endovascular Corporation. The 510(k) number is K083922.

When did MICRUS MICROCATHETER, COURIER FLEX, MODEL MSF 170000-00 receive FDA 510(k) clearance?

MICRUS MICROCATHETER, COURIER FLEX, MODEL MSF 170000-00 received FDA 510(k) clearance on 2009-05-06, under 510(k) number K083922.

Who is the listed applicant for MICRUS MICROCATHETER, COURIER FLEX, MODEL MSF 170000-00?

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 MICROCATHETER, COURIER FLEX, MODEL MSF 170000-00?

The FDA product code for MICRUS MICROCATHETER, COURIER FLEX, MODEL MSF 170000-00 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.