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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 a medical device manufactured by Vascupatent Medical (Shenzhen) Co., Ltd.. It received FDA 510(k) clearance on 2022-11-07 under approval 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. It is manufactured by Vascupatent Medical (Shenzhen) Co., Ltd.. The 510(k) number is K222679.

When was Vericor Support Catheter approved by the FDA?

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

What company makes Vericor Support Catheter?

Vericor Support Catheter is manufactured by Vascupatent Medical (Shenzhen) Co., Ltd..

What is the FDA product code for Vericor Support Catheter?

The FDA product code for Vericor Support Catheter is KRA.

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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.

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