FDA 510(k)

男性乳胶避孕套HA

K号: K252622 · 2026-05-04

决定日期2026-05-04

产品代码HIS

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决定实质等同

器械摘要

Male Latex Condom HA is the device name listed in this FDA 510(k) record. The listed applicant is Okamoto USA, Inc.. It received FDA 510(k) clearance on 2026-05-04 under 510(k) number K252622. 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 Male Latex Condom HA?

Male Latex Condom HA is a medical device that received FDA 510(k) clearance on 2026-05-04. The listed applicant is Okamoto USA, Inc.. The 510(k) number is K252622.

When did Male Latex Condom HA receive FDA 510(k) clearance?

Male Latex Condom HA received FDA 510(k) clearance on 2026-05-04, under 510(k) number K252622.

Who is the listed applicant for Male Latex Condom HA?

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

What is the FDA product code for Male Latex Condom HA?

The FDA product code for Male Latex Condom HA is HIS.

列明Okamoto USA, 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。

K2435840.04 ZERO ZERO FOUR男性乳胶避孕套 K203541Okamoto 002 润滑聚氨酯男性避孕套 K192669极薄003，零零三

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。

K262108FAMA男性乳胶避孕套 - 水性润滑剂（超薄型）；FAMA男性乳胶避孕套 - 水性润滑剂（普通型）；FAMA男性乳胶避孕套 - 水性润滑剂（肋纹型）；FAMA男性乳胶避孕套 - 水性润滑剂（点状型）；FAMA男性乳胶避孕套 - 水性润滑剂（非规则形状型）；MO男性乳胶避孕套 - 水性润滑剂（超薄型）；MO男性乳胶避孕套 - 水性润滑剂（普通型）；MO男性乳胶避孕套 - 水性润滑剂（肋纹型）；MO男性乳胶避孕套 - 水性润滑剂（点状型）；MOShanghai Personage Hygiene Products Co., Ltd.K252521LifeStyles® HydraFeel天然橡胶乳胶避孕套Suretex Limited K250034天然橡胶乳胶男用避孕套Shaoguan Regenex Pharmaceuticals Co., Ltd.K243421Lelo Hex 润滑天然乳胶安全套Lelo, Inc.K243640特洛伊™超细条纹Ecstasy乳胶避孕套（润滑型）（特洛伊™超细条纹Ecstasy）Church & Dwight Co., Inc.K2435840.04 ZERO ZERO FOUR男性乳胶避孕套Okamoto USA, Inc.

官方来源

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