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FDA 510(k)

鼻翼SpO2感測器

K 號:K171423 · 2017-07-27

申請人Xhale, Inc.
決定日期2017-07-27
產品代碼DQA
諮詢委員會履歷
決定相當於

器材摘要

Nasal Alar SpO2 Sensor is the device name listed in this FDA 510(k) record. The listed applicant is Xhale, Inc.. It received FDA 510(k) clearance on 2017-07-27 under 510(k) number K171423. 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 Nasal Alar SpO2 Sensor?

Nasal Alar SpO2 Sensor is a medical device that received FDA 510(k) clearance on 2017-07-27. The listed applicant is Xhale, Inc.. The 510(k) number is K171423.

When did Nasal Alar SpO2 Sensor receive FDA 510(k) clearance?

Nasal Alar SpO2 Sensor received FDA 510(k) clearance on 2017-07-27, under 510(k) number K171423.

Who is the listed applicant for Nasal Alar SpO2 Sensor?

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

What is the FDA product code for Nasal Alar SpO2 Sensor?

The FDA product code for Nasal Alar SpO2 Sensor is DQA.

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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。

官方來源

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