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FDA 510(k)

AngioVac F18 85

K-Number: K212386 · 2021-09-30

ApplicantAngioDynamics, Inc.
Decision Date2021-09-30
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AngioVac F18 85 is a medical device manufactured by AngioDynamics, Inc.. It received FDA 510(k) clearance on 2021-09-30 under approval number K212386. 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 F18 85?

AngioVac F18 85 is a medical device that received FDA 510(k) clearance on 2021-09-30. It is manufactured by AngioDynamics, Inc.. The 510(k) number is K212386.

When was AngioVac F18 85 approved by the FDA?

AngioVac F18 85 received FDA 510(k) clearance on 2021-09-30, under approval number K212386.

What company makes AngioVac F18 85?

AngioVac F18 85 is manufactured by AngioDynamics, Inc..

What is the FDA product code for AngioVac F18 85?

The FDA product code for AngioVac F18 85 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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