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FDA 510(k)

Versus™ Catheter (VS110-8B)

K-Number: K241851 · 2024-11-25

ApplicantLiquet Medical, Inc.
Decision Date2024-11-25
Product CodeQEY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Versus™ Catheter (VS110-8B) is the device name listed in this FDA 510(k) record. The listed applicant is Liquet Medical, Inc.. It received FDA 510(k) clearance on 2024-11-25 under 510(k) number K241851. The device is classified under product code QEY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Versus™ Catheter (VS110-8B)?

Versus™ Catheter (VS110-8B) is a medical device that received FDA 510(k) clearance on 2024-11-25. The listed applicant is Liquet Medical, Inc.. The 510(k) number is K241851.

When did Versus™ Catheter (VS110-8B) receive FDA 510(k) clearance?

Versus™ Catheter (VS110-8B) received FDA 510(k) clearance on 2024-11-25, under 510(k) number K241851.

Who is the listed applicant for Versus™ Catheter (VS110-8B)?

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

What is the FDA product code for Versus™ Catheter (VS110-8B)?

The FDA product code for Versus™ Catheter (VS110-8B) is QEY.

Other records listing Liquet Medical, 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.

K260149Versus™ Catheter (VS110-9NB)

Related Devices (Code: QEY)

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.

K260149Versus™ Catheter (VS110-9NB)Liquet Medical, Inc.K251318VariFuse Adjustable Infusion CatheterArgon Medical Devices, Inc.K231653BASHIR™ .035 Endovascular Catheter, BASHIR™ S-B .035 Endovascular CatheterThrombolex, Inc.K222095BASHIR Endovascular Catheter Ref. No. 7201, BASHIR S-B Endovascular Catheter, Ref. No. 7101Thrombolex, Inc.K220866EKOS+ Endovascular DeviceBoston ScientificK213422EkoSonic Endovascular Device, EKOS+ Endovascular DeviceBoston Scientific Corporation

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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