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FDA 510(k)

HEADWAY 17 ADVANCED MICROCATHETER

K-Number: K101542 · 2010-08-06

ApplicantMicroVention, Inc.
Decision Date2010-08-06
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEADWAY 17 ADVANCED 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 2010-08-06 under 510(k) number K101542. 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 ADVANCED MICROCATHETER?

HEADWAY 17 ADVANCED MICROCATHETER is a medical device that received FDA 510(k) clearance on 2010-08-06. The listed applicant is MicroVention, Inc.. The 510(k) number is K101542.

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

HEADWAY 17 ADVANCED MICROCATHETER received FDA 510(k) clearance on 2010-08-06, under 510(k) number K101542.

Who is the listed applicant for HEADWAY 17 ADVANCED 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 ADVANCED MICROCATHETER?

The FDA product code for HEADWAY 17 ADVANCED MICROCATHETER is DQY.

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Related Devices (Code: 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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