FDA 510(k)

3F ANGIOPTIC ANGIOGRAPHIC CATHETER

K-Number: K964033 · 1997-05-06

Decision Date1997-05-06

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

3F ANGIOPTIC ANGIOGRAPHIC CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is AngioDynamics, Inc.. It received FDA 510(k) clearance on 1997-05-06 under 510(k) number K964033. 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 3F ANGIOPTIC ANGIOGRAPHIC CATHETER?

3F ANGIOPTIC ANGIOGRAPHIC CATHETER is a medical device that received FDA 510(k) clearance on 1997-05-06. The listed applicant is AngioDynamics, Inc.. The 510(k) number is K964033.

When did 3F ANGIOPTIC ANGIOGRAPHIC CATHETER receive FDA 510(k) clearance?

3F ANGIOPTIC ANGIOGRAPHIC CATHETER received FDA 510(k) clearance on 1997-05-06, under 510(k) number K964033.

Who is the listed applicant for 3F ANGIOPTIC ANGIOGRAPHIC CATHETER?

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 3F ANGIOPTIC ANGIOGRAPHIC CATHETER?

The FDA product code for 3F ANGIOPTIC 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.