FDA 510(k)

NxStage PureFlow Solution

K号: K233213 · 2024-01-18

决定日期2024-01-18

产品代码KPO

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决定实质等同

器械摘要

NxStage PureFlow Solution is the device name listed in this FDA 510(k) record. The listed applicant is Nxstage Medical, Inc.. It received FDA 510(k) clearance on 2024-01-18 under 510(k) number K233213. The device is classified under product code KPO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the NxStage PureFlow Solution?

NxStage PureFlow Solution is a medical device that received FDA 510(k) clearance on 2024-01-18. The listed applicant is Nxstage Medical, Inc.. The 510(k) number is K233213.

When did NxStage PureFlow Solution receive FDA 510(k) clearance?

NxStage PureFlow Solution received FDA 510(k) clearance on 2024-01-18, under 510(k) number K233213.

Who is the listed applicant for NxStage PureFlow Solution?

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

What is the FDA product code for NxStage PureFlow Solution?

The FDA product code for NxStage PureFlow Solution is KPO.

列明Nxstage Medical, 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。

K232803NxStage System One with Cartridge Express (CAR-170-E and CAR-172-E)K230632VersiHD 配合 GuideMe 软件 K183158NxStage Cartridge Express with Speedswap K181991NxStage Connected Health System K171331NxStage System One K170469NxStage System One Plus

查看所有 7 个设备 →

相关器械（代码：KPO）

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。

官方来源

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