FDA 510(k)

Seidmon Antegrade AQ Stent Set

K-Number: K180216 · 2018-09-28

Decision Date2018-09-28

Product CodeFAD

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

Seidmon Antegrade AQ Stent Set is a medical device manufactured by Cook Incorporated. It received FDA 510(k) clearance on 2018-09-28 under approval number K180216. The device is classified under product code FAD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Seidmon Antegrade AQ Stent Set?

Seidmon Antegrade AQ Stent Set is a medical device that received FDA 510(k) clearance on 2018-09-28. It is manufactured by Cook Incorporated. The 510(k) number is K180216.

When was Seidmon Antegrade AQ Stent Set approved by the FDA?

Seidmon Antegrade AQ Stent Set received FDA 510(k) clearance on 2018-09-28, under approval number K180216.

What company makes Seidmon Antegrade AQ Stent Set?

Seidmon Antegrade AQ Stent Set is manufactured by Cook Incorporated.

What is the FDA product code for Seidmon Antegrade AQ Stent Set?

The FDA product code for Seidmon Antegrade AQ Stent Set is FAD.

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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.