Intera 补充包
K号: K213823 · 2022-03-16
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决定日期2022-03-16
产品代码PTI
咨询委员会医疗设备监管文本翻译如下：
HO
请注意，由于您没有提供具体的医疗设备监管文本内容，以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
决定实质等同
器械摘要
Intera Refill Kit is the device name listed in this FDA 510(k) record. The listed applicant is Intera Oncology, Inc.. It received FDA 510(k) clearance on 2022-03-16 under 510(k) number K213823. The device is classified under product code PTI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Intera Refill Kit?
Intera Refill Kit is a medical device that received FDA 510(k) clearance on 2022-03-16. The listed applicant is Intera Oncology, Inc.. The 510(k) number is K213823.
When did Intera Refill Kit receive FDA 510(k) clearance?
Intera Refill Kit received FDA 510(k) clearance on 2022-03-16, under 510(k) number K213823.
Who is the listed applicant for Intera Refill Kit?
The FDA 510(k) record lists Intera Oncology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Intera Refill Kit?
The FDA product code for Intera Refill Kit is PTI.
相关临床试验
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列明Intera Oncology, 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。
相关器械（代码：PTI）
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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