FDA 510(k)

Invacare® Solara® 3G 和 Solara® 3G Spree 手动轮椅

K号: K181090 · 2018-11-14

决定日期2018-11-14

产品代码IOR

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决定实质等同

器械摘要

Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corporation. It received FDA 510(k) clearance on 2018-11-14 under 510(k) number K181090. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs?

Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs is a medical device that received FDA 510(k) clearance on 2018-11-14. The listed applicant is Invacare Corporation. The 510(k) number is K181090.

When did Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs receive FDA 510(k) clearance?

Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs received FDA 510(k) clearance on 2018-11-14, under 510(k) number K181090.

Who is the listed applicant for Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs?

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

What is the FDA product code for Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs?

The FDA product code for Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs is IOR.

列明Invacare Corporation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。

K203210Invacare Platinum 5NXG 氧气浓缩器 K202379Invacare AVIVA Storm RX 动力轮椅 K200890Invacare Perfecto2V 氧气浓缩器 K192216Invacare AVIVA FX 动力轮椅，型号：IFX-20MP K191159单电池组浓缩器，带肩带携带包，背包肩带，A，POC1 USB 蓝牙适配器，POC1 Invacare 移动医疗应用程序配件，用于 iOS 和 Android 设备，Invacare Platinum 移动制氧机带连接功能 K182946Invacare TDX SP2-HD 配有船长座椅

查看所有 14 个设备 →

官方来源

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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。