FDA 510(k)

麥昆SpO2感測器

K 號：K231979 · 2024-08-16

申請人Shenzhen Mecun Medical Supply Co., Ltd.

決定日期2024-08-16

產品代碼DQA

諮詢委員會履歷

決定相當於

器材摘要

Mecun SpO2 sensor is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Mecun Medical Supply Co., Ltd.. It received FDA 510(k) clearance on 2024-08-16 under 510(k) number K231979. 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 Mecun SpO2 sensor?

Mecun SpO2 sensor is a medical device that received FDA 510(k) clearance on 2024-08-16. The listed applicant is Shenzhen Mecun Medical Supply Co., Ltd.. The 510(k) number is K231979.

When did Mecun SpO2 sensor receive FDA 510(k) clearance?

Mecun SpO2 sensor received FDA 510(k) clearance on 2024-08-16, under 510(k) number K231979.

Who is the listed applicant for Mecun SpO2 sensor?

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

What is the FDA product code for Mecun SpO2 sensor?

The FDA product code for Mecun SpO2 sensor is DQA.

其他以 Shenzhen Mecun Medical Supply 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。

K231985一次性接地垫 K232460一次性電外科筆（MD1000）

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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