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FDA 510(k)

CHAPERON GUIDING CATHETER

K-Number: K082385 · 2008-12-11

ApplicantMicroVention, Inc.
Decision Date2008-12-11
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CHAPERON GUIDING CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is MicroVention, Inc.. It received FDA 510(k) clearance on 2008-12-11 under 510(k) number K082385. 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 CHAPERON GUIDING CATHETER?

CHAPERON GUIDING CATHETER is a medical device that received FDA 510(k) clearance on 2008-12-11. The listed applicant is MicroVention, Inc.. The 510(k) number is K082385.

When did CHAPERON GUIDING CATHETER receive FDA 510(k) clearance?

CHAPERON GUIDING CATHETER received FDA 510(k) clearance on 2008-12-11, under 510(k) number K082385.

Who is the listed applicant for CHAPERON GUIDING CATHETER?

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 CHAPERON GUIDING CATHETER?

The FDA product code for CHAPERON GUIDING CATHETER is DQY.

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Related Devices (Code: DQY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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