FDA 510(k)

Unity 皮下给药系统（Remodulin）

K号: K190182 · 2019-05-06

决定日期2019-05-06

产品代码FRN

咨询委员会医疗设备监管文本翻译如下： HO 请注意，由于您没有提供具体的医疗设备监管文本内容，以上仅为示例。请提供具体的文本内容以便进行准确的翻译。

决定实质等同

器械摘要

Unity Subcutaneous Delivery System for Remodulin is the device name listed in this FDA 510(k) record. The listed applicant is DEKA Research & Development. It received FDA 510(k) clearance on 2019-05-06 under 510(k) number K190182. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Unity Subcutaneous Delivery System for Remodulin?

Unity Subcutaneous Delivery System for Remodulin is a medical device that received FDA 510(k) clearance on 2019-05-06. The listed applicant is DEKA Research & Development. The 510(k) number is K190182.

When did Unity Subcutaneous Delivery System for Remodulin receive FDA 510(k) clearance?

Unity Subcutaneous Delivery System for Remodulin received FDA 510(k) clearance on 2019-05-06, under 510(k) number K190182.

Who is the listed applicant for Unity Subcutaneous Delivery System for Remodulin?

The FDA 510(k) record lists DEKA Research & Development as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Unity Subcutaneous Delivery System for Remodulin?

The FDA product code for Unity Subcutaneous Delivery System for Remodulin is FRN.

列明DEKA Research & Development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。

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相关器械（代码：FRN）

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。

K253703RemunityPRO+ Remodulin®（曲前列尼尔）注射泵Deka R&D Corp K252015FreedomEdge输液系统；高流量SubQ注射针套装；精确流量管Koru Medical Systems, Inc.K251636Spectrum IQ 注射系统，配备剂量 IQ 安全软件（3570009）Baxter Healthcare Corporation K251640SIGMA Spectrum 输液泵带主药物库Baxter Healthcare Corporation K242752MRidium 3870 MRI输液泵系统（3870）Iradimed Corporation K243855BD Alaris 输液系统带Guardrails Suite MXCarefusion 303, Inc.

官方来源

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