FDA 510(k)

歐蘭帕克口罩

K 號：K230476 · 2023-10-19

申請人Resmed Pty Ltd (Registration Number: 3004604967)

決定日期2023-10-19

產品代碼BZD

諮詢委員會AN

決定相當於

器材摘要

Oran Park Mask is the device name listed in this FDA 510(k) record. The listed applicant is Resmed Pty Ltd (Registration Number: 3004604967). It received FDA 510(k) clearance on 2023-10-19 under 510(k) number K230476. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Oran Park Mask?

Oran Park Mask is a medical device that received FDA 510(k) clearance on 2023-10-19. The listed applicant is Resmed Pty Ltd (Registration Number: 3004604967). The 510(k) number is K230476.

When did Oran Park Mask receive FDA 510(k) clearance?

Oran Park Mask received FDA 510(k) clearance on 2023-10-19, under 510(k) number K230476.

Who is the listed applicant for Oran Park Mask?

The FDA 510(k) record lists Resmed Pty Ltd (Registration Number: 3004604967) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Oran Park Mask?

The FDA product code for Oran Park Mask is BZD.

其他以 Resmed Pty Ltd (Registration Number: 3004604967) 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。

K234134AirFit F30i 面罩系統; AirFit F30i NM 面罩系統; Arcadia 面罩系統 K223747維多尼亞口罩系統

相關器械（代碼：BZD）

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。

K261262Altis 全面罩Respironics, Inc.K253044RXiBreeze PAP系統（RXiBreeze 20C）Resvent Medical Technology Co., Ltd.K253553歐里安Resmed Corp K254104ResScan 基礎版Resmed Corp K251920睡眠呼吸中止症呼吸治療面罩：JoyMask 20-B 全面罩，JoyMask 21-B 全面罩Dcstar, Inc.K253166F6S 全面罩 (F6S)；P6S 鼻枕接口 (P6S)BMC Medical Co., Ltd.

官方來源

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