MuscleView
K号: K241331 · 2024-10-01
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器械摘要
MuscleView is the device name listed in this FDA 510(k) record. The listed applicant is Springbok, Inc.. It received FDA 510(k) clearance on 2024-10-01 under 510(k) number K241331. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MuscleView?
MuscleView is a medical device that received FDA 510(k) clearance on 2024-10-01. The listed applicant is Springbok, Inc.. The 510(k) number is K241331.
When did MuscleView receive FDA 510(k) clearance?
MuscleView received FDA 510(k) clearance on 2024-10-01, under 510(k) number K241331.
Who is the listed applicant for MuscleView?
The FDA 510(k) record lists Springbok, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MuscleView?
The FDA product code for MuscleView is LNH.
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相关器械（代码：LNH）
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
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