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FDA 510(k)

LimFlow V-Ceiver

K-Number: K222083 · 2022-08-09

ApplicantLimFlow, Inc.
Decision Date2022-08-09
Product CodeMMX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LimFlow V-Ceiver is the device name listed in this FDA 510(k) record. The listed applicant is LimFlow, Inc.. It received FDA 510(k) clearance on 2022-08-09 under 510(k) number K222083. 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 LimFlow V-Ceiver?

LimFlow V-Ceiver is a medical device that received FDA 510(k) clearance on 2022-08-09. The listed applicant is LimFlow, Inc.. The 510(k) number is K222083.

When did LimFlow V-Ceiver receive FDA 510(k) clearance?

LimFlow V-Ceiver received FDA 510(k) clearance on 2022-08-09, under 510(k) number K222083.

Who is the listed applicant for LimFlow V-Ceiver?

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 V-Ceiver?

The FDA product code for LimFlow V-Ceiver is MMX.

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 VectorPMA P220025Stent graft, infrapopliteal, venous arterializationK251376LimFlow ARCK242776LimFlow V-CeiverK221902LimFlow VectorK221541LimFlow ARC

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Related Devices (Code: MMX)

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.

K242776LimFlow V-CeiverLimFlow, Inc.K241259Amplatz Goose Neck Snare KitMedtronic, Inc.K232443Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval KitArgon Medical Devices, Inc.K222254Gunther Tulip Vena Cava Filter Retrieval SetCook IncorporatedK212988ONO Retrieval DeviceOnocor Vascular, LLCK213494Aveir Retrieval CatheterABBOTT MEDICAL

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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