Orfit 悬挂式床
K号: K200282 · 2020-04-08
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器械摘要
Orfit Aerial Couchtop is the device name listed in this FDA 510(k) record. The listed applicant is Orfit Industries NV. It received FDA 510(k) clearance on 2020-04-08 under 510(k) number K200282. The device is classified under product code LHN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Orfit Aerial Couchtop?
Orfit Aerial Couchtop is a medical device that received FDA 510(k) clearance on 2020-04-08. The listed applicant is Orfit Industries NV. The 510(k) number is K200282.
When did Orfit Aerial Couchtop receive FDA 510(k) clearance?
Orfit Aerial Couchtop received FDA 510(k) clearance on 2020-04-08, under 510(k) number K200282.
Who is the listed applicant for Orfit Aerial Couchtop?
The FDA 510(k) record lists Orfit Industries NV as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Orfit Aerial Couchtop?
The FDA product code for Orfit Aerial Couchtop is LHN.
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Orfit Industries NV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：LHN）
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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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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