FDA 510(k)

手持式血氧濃度計

K 號：K213431 · 2023-02-26

申請人Shenzhen Witleaf Medical Electronics Co., Ltd.

決定日期2023-02-26

產品代碼DQA

諮詢委員會履歷

決定相當於

器材摘要

Handheld Pulse Oximeter is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Witleaf Medical Electronics Co., Ltd.. It received FDA 510(k) clearance on 2023-02-26 under 510(k) number K213431. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Handheld Pulse Oximeter?

Handheld Pulse Oximeter is a medical device that received FDA 510(k) clearance on 2023-02-26. The listed applicant is Shenzhen Witleaf Medical Electronics Co., Ltd.. The 510(k) number is K213431.

When did Handheld Pulse Oximeter receive FDA 510(k) clearance?

Handheld Pulse Oximeter received FDA 510(k) clearance on 2023-02-26, under 510(k) number K213431.

Who is the listed applicant for Handheld Pulse Oximeter?

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

What is the FDA product code for Handheld Pulse Oximeter?

The FDA product code for Handheld Pulse Oximeter is DQA.

其他以 Shenzhen Witleaf Medical Electronics Co., Ltd. 為申請人之記錄

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。

K213430指尖血氧計

相關器械（代碼：DQA）

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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官方來源

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