FDA 510(k)

无菌聚氯乙烯检查手套，无粉

K号: K170612 · 2017-10-23

决定日期2017-10-23

产品代码LYZ

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

STERILE VINYL EXAMINATION GLOVES, Powder Free is the device name listed in this FDA 510(k) record. The listed applicant is Primus Gloves Pvt Limited. It received FDA 510(k) clearance on 2017-10-23 under 510(k) number K170612. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the STERILE VINYL EXAMINATION GLOVES, Powder Free?

STERILE VINYL EXAMINATION GLOVES, Powder Free is a medical device that received FDA 510(k) clearance on 2017-10-23. The listed applicant is Primus Gloves Pvt Limited. The 510(k) number is K170612.

When did STERILE VINYL EXAMINATION GLOVES, Powder Free receive FDA 510(k) clearance?

STERILE VINYL EXAMINATION GLOVES, Powder Free received FDA 510(k) clearance on 2017-10-23, under 510(k) number K170612.

Who is the listed applicant for STERILE VINYL EXAMINATION GLOVES, Powder Free?

The FDA 510(k) record lists Primus Gloves Pvt Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERILE VINYL EXAMINATION GLOVES, Powder Free?

The FDA product code for STERILE VINYL EXAMINATION GLOVES, Powder Free is LYZ.

列明Primus Gloves Pvt Limited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。

K170515无菌乳胶粉无手术手套，无粉 K143477无粉丁腈患者检查手套，蓝色

官方来源

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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。