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FDA 510(k)

HEADWAY 17 MICROCATHETER

K-Number: K083343 · 2008-12-04

ApplicantMicroVention, Inc.
Decision Date2008-12-04
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEADWAY 17 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 2008-12-04 under 510(k) number K083343. 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 17 MICROCATHETER?

HEADWAY 17 MICROCATHETER is a medical device that received FDA 510(k) clearance on 2008-12-04. The listed applicant is MicroVention, Inc.. The 510(k) number is K083343.

When did HEADWAY 17 MICROCATHETER receive FDA 510(k) clearance?

HEADWAY 17 MICROCATHETER received FDA 510(k) clearance on 2008-12-04, under 510(k) number K083343.

Who is the listed applicant for HEADWAY 17 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 17 MICROCATHETER?

The FDA product code for HEADWAY 17 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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