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FDA 510(k)

Aveir Retrieval Catheter

K-Number: K213494 · 2022-04-01

ApplicantABBOTT MEDICAL
Decision Date2022-04-01
Product CodeMMX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Aveir Retrieval Catheter is a medical device manufactured by ABBOTT MEDICAL. It received FDA 510(k) clearance on 2022-04-01 under approval number K213494. The device is classified under product code MMX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Aveir Retrieval Catheter?

Aveir Retrieval Catheter is a medical device that received FDA 510(k) clearance on 2022-04-01. It is manufactured by ABBOTT MEDICAL. The 510(k) number is K213494.

When was Aveir Retrieval Catheter approved by the FDA?

Aveir Retrieval Catheter received FDA 510(k) clearance on 2022-04-01, under approval number K213494.

What company makes Aveir Retrieval Catheter?

Aveir Retrieval Catheter is manufactured by ABBOTT MEDICAL.

What is the FDA product code for Aveir Retrieval Catheter?

The FDA product code for Aveir Retrieval Catheter is MMX.

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Related Devices (Code: MMX)

K160593Indy OTW Vascular RetrieverCook Incorporated K152136Recovery Cone Removal SystemC.R. Bard, Inc. K170987Captus Vascular Retrieval SystemAvantec Vascular Corporation K163307Expro Elite Snare, Sympro Elite SnareVascular Solutions, Inc. K181757Günther Tulip® Vena Cava Filter Retrieval SetCook Incorporated K191758Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval KitArgon Medical Devices, Inc.

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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