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FDA 510(k)

Vericor Support Catheter

K-Number: K222679 · 2022-11-07

ApplicantVascupatent Medical (Shenzhen) Co., Ltd.
Decision Date2022-11-07
Product CodeKRA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Vericor Support Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Vascupatent Medical (Shenzhen) Co., Ltd.. It received FDA 510(k) clearance on 2022-11-07 under 510(k) number K222679. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Vericor Support Catheter?

Vericor Support Catheter is a medical device that received FDA 510(k) clearance on 2022-11-07. The listed applicant is Vascupatent Medical (Shenzhen) Co., Ltd.. The 510(k) number is K222679.

When did Vericor Support Catheter receive FDA 510(k) clearance?

Vericor Support Catheter received FDA 510(k) clearance on 2022-11-07, under 510(k) number K222679.

Who is the listed applicant for Vericor Support Catheter?

The FDA 510(k) record lists Vascupatent Medical (Shenzhen) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vericor Support Catheter?

The FDA product code for Vericor Support Catheter is KRA.

Related Devices (Code: KRA)

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.

K261610Verge™ MicrocatheterInstylla, Inc.K260771TruSelect™ 2.6 MicrocatheterBoston Scientific CorporationK250794InVera Infusion DeviceInvera MedicalK243534Micro CatheterSuzhou Zenith Vascular SciTech LimitedK231821XO Cath Microcatheter (E20-090-S, E20-110-S, E20-130-S, E20-150-S, E20-175-S, E20-220-S, E20-090-B, E20-110-B, E20-130-B, E20-150-B, E20-175-B, E20-220-B, E26-090-S, E26-110-S, E26-130-S, E26-150-S, E26-175-S, E26-220-S, E26-090-B, E26-110-B, E26-130-B, E26-150-B, E26-175-B, E26-220-B,)Transit Scientific, LLCK231279Peregrine System Infusion Catheter 4-7 mm, Peregrine System Infusion Catheter 3-4 mmAblative Solutions, 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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