MySegmenter（v2.0.0）
K号: K242647 · 2025-04-16
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器械摘要
MySegmenter (v2.0.0) is the device name listed in this FDA 510(k) record. The listed applicant is Mysegmenter Technologies, Inc.. It received FDA 510(k) clearance on 2025-04-16 under 510(k) number K242647. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MySegmenter (v2.0.0)?
MySegmenter (v2.0.0) is a medical device that received FDA 510(k) clearance on 2025-04-16. The listed applicant is Mysegmenter Technologies, Inc.. The 510(k) number is K242647.
When did MySegmenter (v2.0.0) receive FDA 510(k) clearance?
MySegmenter (v2.0.0) received FDA 510(k) clearance on 2025-04-16, under 510(k) number K242647.
Who is the listed applicant for MySegmenter (v2.0.0)?
The FDA 510(k) record lists Mysegmenter Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MySegmenter (v2.0.0)?
The FDA product code for MySegmenter (v2.0.0) is LLZ.
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相关器械（代码：LLZ）
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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