FDA 510(k)

1.5T 24E Posterior Array

K-Number: K223203 · 2023-03-02

Decision Date2023-03-02

Product CodeLNH

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

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

When was 1.5T 24E Posterior Array approved by the FDA?

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

What company makes 1.5T 24E Posterior Array?

1.5T 24E Posterior Array is manufactured by Shenzhen RF Tech Co., Ltd..

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

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

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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.