ProSeal™ 注射部位延长型雄性鲁尔锁 (422140)
K号: K240433 · 2024-05-21
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器械摘要
常见问题
What is the ProSeal™ Injection Site Extended Male Luer Lock (422140)?
ProSeal™ Injection Site Extended Male Luer Lock (422140) is a medical device that received FDA 510(k) clearance on 2024-05-21. The listed applicant is Epic Medical Pte. , Ltd.. The 510(k) number is K240433.
When did ProSeal™ Injection Site Extended Male Luer Lock (422140) receive FDA 510(k) clearance?
ProSeal™ Injection Site Extended Male Luer Lock (422140) received FDA 510(k) clearance on 2024-05-21, under 510(k) number K240433.
Who is the listed applicant for ProSeal™ Injection Site Extended Male Luer Lock (422140)?
The FDA 510(k) record lists Epic Medical Pte. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ProSeal™ Injection Site Extended Male Luer Lock (422140)?
The FDA product code for ProSeal™ Injection Site Extended Male Luer Lock (422140) is ONB.
相关临床试验
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列明Epic Medical Pte. , 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：ONB）
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
在 FDA 数据库中查看 →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。
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