FDA 510(k)

MEDRAD VANGUARD DX ANGIOGRAPHIC CATHETER

K-Number: K050371 · 2005-06-07

Decision Date2005-06-07

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MEDRAD VANGUARD DX ANGIOGRAPHIC CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Medrad, Inc.. It received FDA 510(k) clearance on 2005-06-07 under 510(k) number K050371. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDRAD VANGUARD DX ANGIOGRAPHIC CATHETER?

MEDRAD VANGUARD DX ANGIOGRAPHIC CATHETER is a medical device that received FDA 510(k) clearance on 2005-06-07. The listed applicant is Medrad, Inc.. The 510(k) number is K050371.

When did MEDRAD VANGUARD DX ANGIOGRAPHIC CATHETER receive FDA 510(k) clearance?

MEDRAD VANGUARD DX ANGIOGRAPHIC CATHETER received FDA 510(k) clearance on 2005-06-07, under 510(k) number K050371.

Who is the listed applicant for MEDRAD VANGUARD DX ANGIOGRAPHIC CATHETER?

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

What is the FDA product code for MEDRAD VANGUARD DX ANGIOGRAPHIC CATHETER?

The FDA product code for MEDRAD VANGUARD DX ANGIOGRAPHIC CATHETER is DQO.

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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.