Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LimFlow Vector

K-Number: K221902 · 2022-12-21

ApplicantLimFlow, Inc.
Decision Date2022-12-21
Product CodeMGZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LimFlow Vector is a medical device manufactured by LimFlow, Inc.. It received FDA 510(k) clearance on 2022-12-21 under approval 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. It is manufactured by LimFlow, Inc.. The 510(k) number is K221902.

When was LimFlow Vector approved by the FDA?

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

What company makes LimFlow Vector?

LimFlow Vector is manufactured by LimFlow, Inc..

What is the FDA product code for LimFlow Vector?

The FDA product code for LimFlow Vector is MGZ.

Other Devices by LimFlow, Inc.

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

View all 7 devices →

Related Devices (Code: MGZ)

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

↑