FDA 510(k)

MICRUS MICROCATHETER, MODEL COURIER 270

K-Number: K092702 · 2009-11-20

ApplicantMicrus Endovascular Corporation

Decision Date2009-11-20

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MICRUS MICROCATHETER, MODEL COURIER 270 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 2009-11-20 under 510(k) number K092702. 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, MODEL COURIER 270?

MICRUS MICROCATHETER, MODEL COURIER 270 is a medical device that received FDA 510(k) clearance on 2009-11-20. The listed applicant is Micrus Endovascular Corporation. The 510(k) number is K092702.

When did MICRUS MICROCATHETER, MODEL COURIER 270 receive FDA 510(k) clearance?

MICRUS MICROCATHETER, MODEL COURIER 270 received FDA 510(k) clearance on 2009-11-20, under 510(k) number K092702.

Who is the listed applicant for MICRUS MICROCATHETER, MODEL COURIER 270?

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, MODEL COURIER 270?

The FDA product code for MICRUS MICROCATHETER, MODEL COURIER 270 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.