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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 the device name listed in this FDA 510(k) record. The listed applicant is AngioDynamics, Inc.. It received FDA 510(k) clearance on 2021-09-30 under 510(k) 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. The listed applicant is AngioDynamics, Inc.. The 510(k) number is K212386.

When did AngioVac F18 85 receive FDA 510(k) clearance?

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

Who is the listed applicant for AngioVac F18 85?

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 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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