FDA 510(k)

LimFlow Vector

K-Number: K221902 · 2022-12-21

Decision Date2022-12-21

Product CodeMGZ

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

LimFlow Vector is the device name listed in this FDA 510(k) record. The listed applicant is LimFlow, Inc.. It received FDA 510(k) clearance on 2022-12-21 under 510(k) number K221902. The device is classified under product code MGZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LimFlow Vector?

LimFlow Vector is a medical device that received FDA 510(k) clearance on 2022-12-21. The listed applicant is LimFlow, Inc.. The 510(k) number is K221902.

When did LimFlow Vector receive FDA 510(k) clearance?

LimFlow Vector received FDA 510(k) clearance on 2022-12-21, under 510(k) number K221902.

Who is the listed applicant for LimFlow Vector?

The FDA 510(k) record lists LimFlow, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LimFlow Vector?

The FDA product code for LimFlow Vector is MGZ.

Other records listing LimFlow, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260188LimFlow Vector PMA P220025Stent graft, infrapopliteal, venous arterialization K251376LimFlow ARC K242776LimFlow V-Ceiver K221541LimFlow ARC K222083LimFlow V-Ceiver

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Related Devices (Code: MGZ)

K260188LimFlow VectorLimFlow, Inc.K250105Boomerang Valvulotome (BMGVT080); Boomerang Push Valvulotome (BMGPVT125)Aveera Medical, Inc.K190267EZE SIT ValvulotomeLemaitre Vascular

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.