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FDA 510(k)

1.5T 24E Posterior Array

K-Number: K223203 · 2023-03-02

ApplicantShenzhen RF Tech Co., Ltd.
Decision Date2023-03-02
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

1.5T 24E Posterior Array is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen RF Tech Co., Ltd.. It received FDA 510(k) clearance on 2023-03-02 under 510(k) number K223203. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 1.5T 24E Posterior Array?

1.5T 24E Posterior Array is a medical device that received FDA 510(k) clearance on 2023-03-02. The listed applicant is Shenzhen RF Tech Co., Ltd.. The 510(k) number is K223203.

When did 1.5T 24E Posterior Array receive FDA 510(k) clearance?

1.5T 24E Posterior Array received FDA 510(k) clearance on 2023-03-02, under 510(k) number K223203.

Who is the listed applicant for 1.5T 24E Posterior Array?

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

What is the FDA product code for 1.5T 24E Posterior Array?

The FDA product code for 1.5T 24E Posterior Array is LNH.

Other records listing Shenzhen RF Tech Co., Ltd. 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.

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Related Devices (Code: LNH)

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.

K253808AIR Recon DLGE Medical SystemsK261331I-Genius (100019400)Esaote, S.p.A.K260852MAGNETOM Flow.Elite;MAGNETOM Flow.Neo;MAGNETOM Flow.Rise;MAGNETOM Flow.PureSiemens Healthineers AGK260113uMR AstraShanghai United Imaging Healthcare Co., Ltd.K253862APERTO Lucent MRI SystemFujifilm CorporationK260746S-scan Open (100001800)Esaote, S.p.A.

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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