FDA 510(k)

MEDTRONIC ANGIOGRAPHIC GUIDE WIRES

K-Number: K082873 · 2009-02-06

Decision Date2009-02-06

Product CodeDQX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MEDTRONIC ANGIOGRAPHIC GUIDE WIRES is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 2009-02-06 under 510(k) number K082873. 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 MEDTRONIC ANGIOGRAPHIC GUIDE WIRES?

MEDTRONIC ANGIOGRAPHIC GUIDE WIRES is a medical device that received FDA 510(k) clearance on 2009-02-06. The listed applicant is Medtronic Vascular. The 510(k) number is K082873.

When did MEDTRONIC ANGIOGRAPHIC GUIDE WIRES receive FDA 510(k) clearance?

MEDTRONIC ANGIOGRAPHIC GUIDE WIRES received FDA 510(k) clearance on 2009-02-06, under 510(k) number K082873.

Who is the listed applicant for MEDTRONIC ANGIOGRAPHIC GUIDE WIRES?

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

What is the FDA product code for MEDTRONIC ANGIOGRAPHIC GUIDE WIRES?

The FDA product code for MEDTRONIC ANGIOGRAPHIC GUIDE WIRES is DQX.

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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.