EndoTool SubQ
K号: K180366 · 2018-09-20
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决定日期2018-09-20
产品代码NDC
咨询委员会AN
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器械摘要
EndoTool SubQ is the device name listed in this FDA 510(k) record. The listed applicant is Al Pacheco and Associates. It received FDA 510(k) clearance on 2018-09-20 under 510(k) number K180366. The device is classified under product code NDC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the EndoTool SubQ?
EndoTool SubQ is a medical device that received FDA 510(k) clearance on 2018-09-20. The listed applicant is Al Pacheco and Associates. The 510(k) number is K180366.
When did EndoTool SubQ receive FDA 510(k) clearance?
EndoTool SubQ received FDA 510(k) clearance on 2018-09-20, under 510(k) number K180366.
Who is the listed applicant for EndoTool SubQ?
The FDA 510(k) record lists Al Pacheco and Associates as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EndoTool SubQ?
The FDA product code for EndoTool SubQ is NDC.
相关临床试验
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相关器械（代码：NDC）
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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