L-Cath™ 单双腔导管,L-Cath™ 中线导管
K号: K230669 · 2023-11-30
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器械摘要
常见问题
What is the L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters?
L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters is a medical device that received FDA 510(k) clearance on 2023-11-30. The listed applicant is Argon Medical Devices. The 510(k) number is K230669.
When did L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters receive FDA 510(k) clearance?
L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters received FDA 510(k) clearance on 2023-11-30, under 510(k) number K230669.
Who is the listed applicant for L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters?
The FDA 510(k) record lists Argon Medical Devices as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters?
The FDA product code for L-Cath™ Single and Dual Lumen Catheters, L-Cath™ Midline Catheters is LJS.
相关临床试验
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列明Argon Medical Devices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:LJS)
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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