FDA 510(k)

Silent Nite® 呼吸暂停治疗仪带Glidewell铰链™（SNGLHG）

K号: K233434 · 2023-11-14

决定日期2023-11-14

产品代码LRK

咨询委员会DE 请注意，您没有提供具体的医疗设备监管文本内容，因此我无法进行翻译。请提供需要翻译的具体文本，我将根据您的要求进行翻译。

决定实质等同

器械摘要

Silent Nite® Sleep Appliance with the Glidewell Hinge™ (SNGLHG) is the device name listed in this FDA 510(k) record. The listed applicant is Prismatik Dentalcraft, Inc.. It received FDA 510(k) clearance on 2023-11-14 under 510(k) number K233434. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Silent Nite® Sleep Appliance with the Glidewell Hinge™ (SNGLHG)?

Silent Nite® Sleep Appliance with the Glidewell Hinge™ (SNGLHG) is a medical device that received FDA 510(k) clearance on 2023-11-14. The listed applicant is Prismatik Dentalcraft, Inc.. The 510(k) number is K233434.

When did Silent Nite® Sleep Appliance with the Glidewell Hinge™ (SNGLHG) receive FDA 510(k) clearance?

Silent Nite® Sleep Appliance with the Glidewell Hinge™ (SNGLHG) received FDA 510(k) clearance on 2023-11-14, under 510(k) number K233434.

Who is the listed applicant for Silent Nite® Sleep Appliance with the Glidewell Hinge™ (SNGLHG)?

FDA 510(k)记录将Prismatik Dentalcraft, Inc.列为申请人。这本身并不足以确立该设备的制造商。

What is the FDA product code for Silent Nite® Sleep Appliance with the Glidewell Hinge™ (SNGLHG)?

The FDA product code for Silent Nite® Sleep Appliance with the Glidewell Hinge™ (SNGLHG) is LRK.

列明Prismatik Dentalcraft, Inc.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。

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官方来源

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