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FDA 510(k)

AITRICS-VC

K-Number: K240756 · 2024-07-23

ApplicantAitrics Co., Ltd.
Decision Date2024-07-23
Product CodePLB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AITRICS-VC is the device name listed in this FDA 510(k) record. The listed applicant is Aitrics Co., Ltd.. It received FDA 510(k) clearance on 2024-07-23 under 510(k) number K240756. The device is classified under product code PLB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AITRICS-VC?

AITRICS-VC is a medical device that received FDA 510(k) clearance on 2024-07-23. The listed applicant is Aitrics Co., Ltd.. The 510(k) number is K240756.

When did AITRICS-VC receive FDA 510(k) clearance?

AITRICS-VC received FDA 510(k) clearance on 2024-07-23, under 510(k) number K240756.

Who is the listed applicant for AITRICS-VC?

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

What is the FDA product code for AITRICS-VC?

The FDA product code for AITRICS-VC is PLB.

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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.

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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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