Merlexi Craft肥胖系列手动轮椅
K号: K240120 · 2024-07-05
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器械摘要
常见问题
What is the Merlexi Craft Bariatric series of manual wheelchairs?
Merlexi Craft Bariatric series of manual wheelchairs is a medical device that received FDA 510(k) clearance on 2024-07-05. The listed applicant is Turbo Wheelchair Co., Inc.. The 510(k) number is K240120.
When did Merlexi Craft Bariatric series of manual wheelchairs receive FDA 510(k) clearance?
Merlexi Craft Bariatric series of manual wheelchairs received FDA 510(k) clearance on 2024-07-05, under 510(k) number K240120.
Who is the listed applicant for Merlexi Craft Bariatric series of manual wheelchairs?
The FDA 510(k) record lists Turbo Wheelchair Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Merlexi Craft Bariatric series of manual wheelchairs?
The FDA product code for Merlexi Craft Bariatric series of manual wheelchairs is IOR.
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。
相关器械(代码:IOR)
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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