FDA 510(k)

WiZARD 310/320系列CPAP口罩

K 號：K182394 · 2019-05-17

決定日期2019-05-17

產品代碼BZD

諮詢委員會AN

決定相當於

器材摘要

WiZARD 310/320 Series CPAP Mask is the device name listed in this FDA 510(k) record. The listed applicant is Apex Medical Corp.. It received FDA 510(k) clearance on 2019-05-17 under 510(k) number K182394. 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 WiZARD 310/320 Series CPAP Mask?

WiZARD 310/320 Series CPAP Mask is a medical device that received FDA 510(k) clearance on 2019-05-17. The listed applicant is Apex Medical Corp.. The 510(k) number is K182394.

When did WiZARD 310/320 Series CPAP Mask receive FDA 510(k) clearance?

WiZARD 310/320 Series CPAP Mask received FDA 510(k) clearance on 2019-05-17, under 510(k) number K182394.

Who is the listed applicant for WiZARD 310/320 Series CPAP Mask?

The FDA 510(k) record lists Apex Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WiZARD 310/320 Series CPAP Mask?

The FDA product code for WiZARD 310/320 Series CPAP Mask is BZD.

其他以 Apex Medical Corp. 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。

K213577VenAir，連續壓縮系統 K193206WiZARD 510 鼻罩

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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