MySleepDash
K号: K252338 · 2026-04-17
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决定日期2026-04-17
产品代码BZD
咨询委员会AN
请注意，由于您没有提供完整的医疗设备监管文本，我无法提供完整的翻译。如果您能提供完整的文本，我将很乐意为您翻译。
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器械摘要
MySleepDash is the device name listed in this FDA 510(k) record. The listed applicant is Somnetics International, Inc. (Dba Transcend Inc). It received FDA 510(k) clearance on 2026-04-17 under 510(k) number K252338. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the MySleepDash?
MySleepDash is a medical device that received FDA 510(k) clearance on 2026-04-17. The listed applicant is Somnetics International, Inc. (Dba Transcend Inc). The 510(k) number is K252338.
When did MySleepDash receive FDA 510(k) clearance?
MySleepDash received FDA 510(k) clearance on 2026-04-17, under 510(k) number K252338.
Who is the listed applicant for MySleepDash?
The FDA 510(k) record lists Somnetics International, Inc. (Dba Transcend Inc) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MySleepDash?
The FDA product code for MySleepDash is BZD.
相关临床试验
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相关器械（代码：BZD）
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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