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FDA 510(k)

AngioVac C20, AngioVac C180

K-Number: K190594 · 2019-07-05

ApplicantAngioDynamics, Inc.
Decision Date2019-07-05
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AngioVac C20, AngioVac C180 is the device name listed in this FDA 510(k) record. The listed applicant is AngioDynamics, Inc.. It received FDA 510(k) clearance on 2019-07-05 under 510(k) number K190594. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AngioVac C20, AngioVac C180?

AngioVac C20, AngioVac C180 is a medical device that received FDA 510(k) clearance on 2019-07-05. The listed applicant is AngioDynamics, Inc.. The 510(k) number is K190594.

When did AngioVac C20, AngioVac C180 receive FDA 510(k) clearance?

AngioVac C20, AngioVac C180 received FDA 510(k) clearance on 2019-07-05, under 510(k) number K190594.

Who is the listed applicant for AngioVac C20, AngioVac C180?

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 AngioVac C20, AngioVac C180?

The FDA product code for AngioVac C20, AngioVac C180 is DWF.

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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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