FDA 510(k)

Lelo Hex 润滑天然乳胶安全套

K号: K243421 · 2025-03-07

决定日期2025-03-07

产品代码HIS

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决定实质等同

器械摘要

Lelo Hex Lubricated Natural Rubber Latex Condom is the device name listed in this FDA 510(k) record. The listed applicant is Lelo, Inc.. It received FDA 510(k) clearance on 2025-03-07 under 510(k) number K243421. 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 Lelo Hex Lubricated Natural Rubber Latex Condom?

Lelo Hex Lubricated Natural Rubber Latex Condom is a medical device that received FDA 510(k) clearance on 2025-03-07. The listed applicant is Lelo, Inc.. The 510(k) number is K243421.

When did Lelo Hex Lubricated Natural Rubber Latex Condom receive FDA 510(k) clearance?

Lelo Hex Lubricated Natural Rubber Latex Condom received FDA 510(k) clearance on 2025-03-07, under 510(k) number K243421.

Who is the listed applicant for Lelo Hex Lubricated Natural Rubber Latex Condom?

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

What is the FDA product code for Lelo Hex Lubricated Natural Rubber Latex Condom?

The FDA product code for Lelo Hex Lubricated Natural Rubber Latex Condom is HIS.

列明Lelo, 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。

K162511LELO RESPECT HEX 天然橡胶乳胶避孕套 K160644Lelo Hex 天然乳胶安全套

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。

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官方来源

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