FDA 510(k)

ANGIODYNAMICS SOFT-VU ANGIOGRAPHIC CATHETERS

K-Number: K112452 · 2012-03-30

Decision Date2012-03-30

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

ANGIODYNAMICS SOFT-VU ANGIOGRAPHIC CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is AngioDynamics, Inc.. It received FDA 510(k) clearance on 2012-03-30 under 510(k) number K112452. 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 ANGIODYNAMICS SOFT-VU ANGIOGRAPHIC CATHETERS?

ANGIODYNAMICS SOFT-VU ANGIOGRAPHIC CATHETERS is a medical device that received FDA 510(k) clearance on 2012-03-30. The listed applicant is AngioDynamics, Inc.. The 510(k) number is K112452.

When did ANGIODYNAMICS SOFT-VU ANGIOGRAPHIC CATHETERS receive FDA 510(k) clearance?

ANGIODYNAMICS SOFT-VU ANGIOGRAPHIC CATHETERS received FDA 510(k) clearance on 2012-03-30, under 510(k) number K112452.

Who is the listed applicant for ANGIODYNAMICS SOFT-VU ANGIOGRAPHIC CATHETERS?

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

What is the FDA product code for ANGIODYNAMICS SOFT-VU ANGIOGRAPHIC CATHETERS?

The FDA product code for ANGIODYNAMICS SOFT-VU ANGIOGRAPHIC CATHETERS 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.