FDA 510(k)

重新處理胎兒帶

K 號：K221854 · 2022-08-06

決定日期2022-08-06

產品代碼NLH

諮詢委員會履歷

決定相當於

器材摘要

Reprocesses Umbilical Cable is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Health, LLC. It received FDA 510(k) clearance on 2022-08-06 under 510(k) number K221854. The device is classified under product code NLH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Reprocesses Umbilical Cable?

Reprocesses Umbilical Cable is a medical device that received FDA 510(k) clearance on 2022-08-06. The listed applicant is Innovative Health, LLC. The 510(k) number is K221854.

When did Reprocesses Umbilical Cable receive FDA 510(k) clearance?

Reprocesses Umbilical Cable received FDA 510(k) clearance on 2022-08-06, under 510(k) number K221854.

Who is the listed applicant for Reprocesses Umbilical Cable?

The FDA 510(k) record lists Innovative Health, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Reprocesses Umbilical Cable?

The FDA product code for Reprocesses Umbilical Cable is NLH.

其他以 Innovative Health, LLC 為申請人之記錄

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相關器械（代碼：NLH）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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