FDA 510(k)

RenaPure 結核菌內毒素濾過器

K 號：K231410 · 2023-07-19

決定日期2023-07-19

產品代碼FIP

諮詢委員會GU

決定相當於

器材摘要

RenaPure Endotoxin Retentive Filter is the device name listed in this FDA 510(k) record. The listed applicant is Evoqua Water Technologies, LLC. It received FDA 510(k) clearance on 2023-07-19 under 510(k) number K231410. The device is classified under product code FIP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the RenaPure Endotoxin Retentive Filter?

RenaPure Endotoxin Retentive Filter is a medical device that received FDA 510(k) clearance on 2023-07-19. The listed applicant is Evoqua Water Technologies, LLC. The 510(k) number is K231410.

When did RenaPure Endotoxin Retentive Filter receive FDA 510(k) clearance?

RenaPure Endotoxin Retentive Filter received FDA 510(k) clearance on 2023-07-19, under 510(k) number K231410.

Who is the listed applicant for RenaPure Endotoxin Retentive Filter?

The FDA 510(k) record lists Evoqua Water Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RenaPure Endotoxin Retentive Filter?

The FDA product code for RenaPure Endotoxin Retentive Filter is FIP.

其他以 Evoqua Water Technologies, LLC 為申請人之記錄

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K153784NOSOGARD過濾器

相關器械（代碼：FIP）

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。

K250471AquaC UNO HFresenius Medical Care Renal Therapies Group, LLC K251851DIASAFEplusUS (F00013010)Fresenius Medical Care Renal Therapies Group, LLC K252181AquaAFresenius Medical Care North America K250514UPT系列醫療RO水處理系統Specialty Water Technologies, Inc.K232953AquaBplus; AquaB LITEFresenius Medical Care Renal Therapies Group, LLC K223479AQUAbase nXB.Braun Medical, Inc.

官方來源

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