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FDA 510(k)

非杀精润滑男性乳胶避孕套

K号: K193578 · 2020-08-20

决定日期2020-08-20
产品代码HIS
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决定实质等同

器械摘要

Non-spermicidal Lubricated Male Latex Condom is the device name listed in this FDA 510(k) record. The listed applicant is Global Protection Corp.. It received FDA 510(k) clearance on 2020-08-20 under 510(k) number K193578. The device is classified under product code HIS. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Non-spermicidal Lubricated Male Latex Condom?

Non-spermicidal Lubricated Male Latex Condom is a medical device that received FDA 510(k) clearance on 2020-08-20. The listed applicant is Global Protection Corp.. The 510(k) number is K193578.

When did Non-spermicidal Lubricated Male Latex Condom receive FDA 510(k) clearance?

Non-spermicidal Lubricated Male Latex Condom received FDA 510(k) clearance on 2020-08-20, under 510(k) number K193578.

Who is the listed applicant for Non-spermicidal Lubricated Male Latex Condom?

The FDA 510(k) record lists Global Protection Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Non-spermicidal Lubricated Male Latex Condom?

The FDA product code for Non-spermicidal Lubricated Male Latex Condom is HIS.

相关临床试验

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列明Global Protection Corp.为申报人的其他记录

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相关器械(代码:HIS)

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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