Millenium HX
K号: K192398 · 2019-10-03
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决定日期2019-10-03
产品代码FIP
咨询委员会GU
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决定实质等同
器械摘要
Millenium HX is the device name listed in this FDA 510(k) record. The listed applicant is Mar Cor Purification, Inc.. It received FDA 510(k) clearance on 2019-10-03 under 510(k) number K192398. The device is classified under product code FIP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Millenium HX?
Millenium HX is a medical device that received FDA 510(k) clearance on 2019-10-03. The listed applicant is Mar Cor Purification, Inc.. The 510(k) number is K192398.
When did Millenium HX receive FDA 510(k) clearance?
Millenium HX received FDA 510(k) clearance on 2019-10-03, under 510(k) number K192398.
Who is the listed applicant for Millenium HX?
The FDA 510(k) record lists Mar Cor Purification, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Millenium HX?
The FDA product code for Millenium HX is FIP.
相关临床试验
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
列明Mar Cor Purification, Inc.为申报人的其他记录
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
相关器械（代码：FIP）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
K250471AquaC UNO HFresenius Medical Care Renal Therapies Group, LLCK251851DIASAFEplusUS (F00013010)Fresenius Medical Care Renal Therapies Group, LLCK252181AquaAFresenius Medical Care North AmericaK250514UPT系列医用反渗透纯水处理系统Specialty Water Technologies, Inc.K232953AquaBplus; AquaB LITEFresenius Medical Care Renal Therapies Group, LLCK223479AQUAbase nXB.Braun Medical, Inc.
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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