DiscCath针套
K号: K212328 · 2021-09-26
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决定日期2021-09-26
产品代码BSP
咨询委员会AN
请注意，由于您没有提供完整的医疗设备监管文本，我无法提供完整的翻译。如果您能提供完整的文本，我将很乐意为您翻译。
决定实质等同
器械摘要
DiscCath Needle Set is the device name listed in this FDA 510(k) record. The listed applicant is Disccath, LLC. It received FDA 510(k) clearance on 2021-09-26 under 510(k) number K212328. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the DiscCath Needle Set?
DiscCath Needle Set is a medical device that received FDA 510(k) clearance on 2021-09-26. The listed applicant is Disccath, LLC. The 510(k) number is K212328.
When did DiscCath Needle Set receive FDA 510(k) clearance?
DiscCath Needle Set received FDA 510(k) clearance on 2021-09-26, under 510(k) number K212328.
Who is the listed applicant for DiscCath Needle Set?
The FDA 510(k) record lists Disccath, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DiscCath Needle Set?
The FDA product code for DiscCath Needle Set is BSP.
相关临床试验
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：BSP）
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
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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