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FDA 510(k)

Hillrom 心肺速率監測系統,由 EarlySense 驅動

K 號:K223246 · 2022-11-18

決定日期2022-11-18
產品代碼BZQ
諮詢委員會AN
決定相當於

器材摘要

Hillrom Heart and Respiration Rate Monitoring System powered by EarlySense is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corproration. It received FDA 510(k) clearance on 2022-11-18 under 510(k) number K223246. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Hillrom Heart and Respiration Rate Monitoring System powered by EarlySense?

Hillrom Heart and Respiration Rate Monitoring System powered by EarlySense is a medical device that received FDA 510(k) clearance on 2022-11-18. The listed applicant is Baxter Healthcare Corproration. The 510(k) number is K223246.

When did Hillrom Heart and Respiration Rate Monitoring System powered by EarlySense receive FDA 510(k) clearance?

Hillrom Heart and Respiration Rate Monitoring System powered by EarlySense received FDA 510(k) clearance on 2022-11-18, under 510(k) number K223246.

Who is the listed applicant for Hillrom Heart and Respiration Rate Monitoring System powered by EarlySense?

The FDA 510(k) record lists Baxter Healthcare Corproration as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Hillrom Heart and Respiration Rate Monitoring System powered by EarlySense?

The FDA product code for Hillrom Heart and Respiration Rate Monitoring System powered by EarlySense is BZQ.

相關臨床試驗

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相關器械(代碼:BZQ)

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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