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FDA 510(k)

用于治疗角膜暴露的自粘性磁铁装置

K号: K162258 · 2017-04-28

决定日期2017-04-28
产品代码FRG
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

Self Sealing Sterilization Pouches is the device name listed in this FDA 510(k) record. The listed applicant is Tianchang Jiarui Packaging Material Co., Ltd.. It received FDA 510(k) clearance on 2017-04-28 under 510(k) number K162258. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Self Sealing Sterilization Pouches?

Self Sealing Sterilization Pouches is a medical device that received FDA 510(k) clearance on 2017-04-28. The listed applicant is Tianchang Jiarui Packaging Material Co., Ltd.. The 510(k) number is K162258.

When did Self Sealing Sterilization Pouches receive FDA 510(k) clearance?

Self Sealing Sterilization Pouches received FDA 510(k) clearance on 2017-04-28, under 510(k) number K162258.

Who is the listed applicant for Self Sealing Sterilization Pouches?

The FDA 510(k) record lists Tianchang Jiarui Packaging Material Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Self Sealing Sterilization Pouches?

The FDA product code for Self Sealing Sterilization Pouches is FRG.

相关临床试验

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。

列明Tianchang Jiarui Packaging Material Co., Ltd.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。

相关器械(代码:FRG)

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

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