FDA 510(k)

Hydro-Temp 新生儿皮肤温度探头盖

K号: K191425 · 2020-01-21

决定日期2020-01-21

产品代码FMT

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

Hydro-Temp Neonatal Skin Temperature Probe Cover 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 2020-01-21 under 510(k) number K191425. The device is classified under product code FMT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Hydro-Temp Neonatal Skin Temperature Probe Cover?

Hydro-Temp Neonatal Skin Temperature Probe Cover is a medical device that received FDA 510(k) clearance on 2020-01-21. The listed applicant is Deroyal Industries, Inc.. The 510(k) number is K191425.

When did Hydro-Temp Neonatal Skin Temperature Probe Cover receive FDA 510(k) clearance?

Hydro-Temp Neonatal Skin Temperature Probe Cover received FDA 510(k) clearance on 2020-01-21, under 510(k) number K191425.

Who is the listed applicant for Hydro-Temp Neonatal Skin Temperature Probe Cover?

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 Hydro-Temp Neonatal Skin Temperature Probe Cover?

The FDA product code for Hydro-Temp Neonatal Skin Temperature Probe Cover is FMT.

列明Deroyal Industries, 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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