Endotics
K号: K190669 · 2020-01-03
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决定日期2020-01-03
产品代码FDF
咨询委员会GU
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器械摘要
Endotics is the device name listed in this FDA 510(k) record. The listed applicant is Era Endoscopy S.R.L.. It received FDA 510(k) clearance on 2020-01-03 under 510(k) number K190669. The device is classified under product code FDF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Endotics?
Endotics is a medical device that received FDA 510(k) clearance on 2020-01-03. The listed applicant is Era Endoscopy S.R.L.. The 510(k) number is K190669.
When did Endotics receive FDA 510(k) clearance?
Endotics received FDA 510(k) clearance on 2020-01-03, under 510(k) number K190669.
Who is the listed applicant for Endotics?
The FDA 510(k) record lists Era Endoscopy S.R.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Endotics?
The FDA product code for Endotics is FDF.
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：FDF）
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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