FDA 510(k)

Slinky 尿管

K 號：K231179 · 2023-12-01

決定日期2023-12-01

產品代碼QJP

諮詢委員會履歷

決定相當於

器材摘要

Slinky Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Anoxia Medical, Inc.. It received FDA 510(k) clearance on 2023-12-01 under 510(k) number K231179. The device is classified under product code QJP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Slinky Catheter?

Slinky Catheter is a medical device that received FDA 510(k) clearance on 2023-12-01. The listed applicant is Anoxia Medical, Inc.. The 510(k) number is K231179.

When did Slinky Catheter receive FDA 510(k) clearance?

Slinky Catheter received FDA 510(k) clearance on 2023-12-01, under 510(k) number K231179.

Who is the listed applicant for Slinky Catheter?

The FDA 510(k) record lists Anoxia Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Slinky Catheter?

The FDA product code for Slinky Catheter is QJP.

其他以 Anoxia Medical, Inc. 為申請人之記錄

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K232831Quiver 吸引泵

相關器械（代碼：QJP）

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官方來源

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