FDA 510(k)

Apexロケーター（AL-Pex），Apexロケーター（AL-Pex+）

K番号: K232717 · 2023-12-22

決定日2023-12-22

製品コードLQY

決定大幅同等

医療機器の概要

Apex Locator (AL-Pex), Apex Locator (AL-Pex+) is the device name listed in this FDA 510(k) record. The listed applicant is Changzhou Haili Medical Co., Ltd.. It received FDA 510(k) clearance on 2023-12-22 under 510(k) number K232717. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

よくある質問

What is the Apex Locator (AL-Pex), Apex Locator (AL-Pex+)?

Apex Locator (AL-Pex), Apex Locator (AL-Pex+) is a medical device that received FDA 510(k) clearance on 2023-12-22. The listed applicant is Changzhou Haili Medical Co., Ltd.. The 510(k) number is K232717.

When did Apex Locator (AL-Pex), Apex Locator (AL-Pex+) receive FDA 510(k) clearance?

Apex Locator (AL-Pex), Apex Locator (AL-Pex+) received FDA 510(k) clearance on 2023-12-22, under 510(k) number K232717.

Who is the listed applicant for Apex Locator (AL-Pex), Apex Locator (AL-Pex+)?

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

What is the FDA product code for Apex Locator (AL-Pex), Apex Locator (AL-Pex+)?

The FDA product code for Apex Locator (AL-Pex), Apex Locator (AL-Pex+) is LQY.

公式ソース

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Apexロケーター（AL-Pex），Apexロケーター（AL-Pex+）

医療機器の概要

よくある質問

関連する臨床試験

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