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FDA 510(k)

HEADWAY 27 MICROCATHETER

K-Number: K110813 · 2011-08-05

ApplicantMicroVention, Inc.
Decision Date2011-08-05
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEADWAY 27 MICROCATHETER is the device name listed in this FDA 510(k) record. The listed applicant is MicroVention, Inc.. It received FDA 510(k) clearance on 2011-08-05 under 510(k) number K110813. 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 HEADWAY 27 MICROCATHETER?

HEADWAY 27 MICROCATHETER is a medical device that received FDA 510(k) clearance on 2011-08-05. The listed applicant is MicroVention, Inc.. The 510(k) number is K110813.

When did HEADWAY 27 MICROCATHETER receive FDA 510(k) clearance?

HEADWAY 27 MICROCATHETER received FDA 510(k) clearance on 2011-08-05, under 510(k) number K110813.

Who is the listed applicant for HEADWAY 27 MICROCATHETER?

The FDA 510(k) record lists MicroVention, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEADWAY 27 MICROCATHETER?

The FDA product code for HEADWAY 27 MICROCATHETER is DQY.

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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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