Invacare Platinum 移动氧气浓缩器
K号: K160630 · 2016-09-27
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器械摘要
常见问题
What is the Invacare Platinum Mobile Oxygen Concentrator?
Invacare Platinum Mobile Oxygen Concentrator is a medical device that received FDA 510(k) clearance on 2016-09-27. The listed applicant is Invacare Corporation. The 510(k) number is K160630.
When did Invacare Platinum Mobile Oxygen Concentrator receive FDA 510(k) clearance?
Invacare Platinum Mobile Oxygen Concentrator received FDA 510(k) clearance on 2016-09-27, under 510(k) number K160630.
Who is the listed applicant for Invacare Platinum Mobile Oxygen Concentrator?
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 Platinum Mobile Oxygen Concentrator?
The FDA product code for Invacare Platinum Mobile Oxygen Concentrator is CAW.
相关临床试验
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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。
相关器械(代码:CAW)
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
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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