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FDA 510(k)

HEADWAY 21 MICROCATHETER, MODEL: MC212150S

K-Number: K093160 · 2009-11-05

ApplicantMicroVention, Inc.
Decision Date2009-11-05
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEADWAY 21 MICROCATHETER, MODEL: MC212150S is the device name listed in this FDA 510(k) record. The listed applicant is MicroVention, Inc.. It received FDA 510(k) clearance on 2009-11-05 under 510(k) number K093160. 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 21 MICROCATHETER, MODEL: MC212150S?

HEADWAY 21 MICROCATHETER, MODEL: MC212150S is a medical device that received FDA 510(k) clearance on 2009-11-05. The listed applicant is MicroVention, Inc.. The 510(k) number is K093160.

When did HEADWAY 21 MICROCATHETER, MODEL: MC212150S receive FDA 510(k) clearance?

HEADWAY 21 MICROCATHETER, MODEL: MC212150S received FDA 510(k) clearance on 2009-11-05, under 510(k) number K093160.

Who is the listed applicant for HEADWAY 21 MICROCATHETER, MODEL: MC212150S?

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 21 MICROCATHETER, MODEL: MC212150S?

The FDA product code for HEADWAY 21 MICROCATHETER, MODEL: MC212150S 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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