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FDA 510(k)

BRIVANT GUIDEWIRE

K-Number: K060551 · 2006-06-07

Decision Date2006-06-07
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BRIVANT GUIDEWIRE is the device name listed in this FDA 510(k) record. The listed applicant is Brivant Limited. It received FDA 510(k) clearance on 2006-06-07 under 510(k) number K060551. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRIVANT GUIDEWIRE?

BRIVANT GUIDEWIRE is a medical device that received FDA 510(k) clearance on 2006-06-07. The listed applicant is Brivant Limited. The 510(k) number is K060551.

When did BRIVANT GUIDEWIRE receive FDA 510(k) clearance?

BRIVANT GUIDEWIRE received FDA 510(k) clearance on 2006-06-07, under 510(k) number K060551.

Who is the listed applicant for BRIVANT GUIDEWIRE?

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

What is the FDA product code for BRIVANT GUIDEWIRE?

The FDA product code for BRIVANT GUIDEWIRE is DQX.

Related Clinical Trials

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.

Related Devices (Code: DQX)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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