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FDA 510(k)

DeRoyal 温度监测探头

K号: K200631 · 2020-12-23

决定日期2020-12-23
产品代码FLL
咨询委员会医疗设备监管文本翻译如下: HO 请注意,由于您没有提供具体的医疗设备监管文本内容,以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
决定实质等同

器械摘要

DeRoyal Temperature Monitoring Probe is the device name listed in this FDA 510(k) record. The listed applicant is Deroyal Industries, Inc.. It received FDA 510(k) clearance on 2020-12-23 under 510(k) number K200631. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the DeRoyal Temperature Monitoring Probe?

DeRoyal Temperature Monitoring Probe is a medical device that received FDA 510(k) clearance on 2020-12-23. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K200631.

When did DeRoyal Temperature Monitoring Probe receive FDA 510(k) clearance?

DeRoyal Temperature Monitoring Probe received FDA 510(k) clearance on 2020-12-23, under 510(k) number K200631.

Who is the listed applicant for DeRoyal Temperature Monitoring Probe?

The FDA 510(k) record lists Deroyal Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DeRoyal Temperature Monitoring Probe?

The FDA product code for DeRoyal Temperature Monitoring Probe is FLL.

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列明Deroyal Industries, Inc.为申报人的其他记录

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相关器械(代码:FLL)

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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