Absoanchor 微植入
K号: K181142 · 2019-02-05
广告
申请人Dentos, Inc.
决定日期2019-02-05
产品代码OAT
咨询委员会DE
请注意，您没有提供具体的医疗设备监管文本内容，因此我无法进行翻译。请提供需要翻译的具体文本，我将根据您的要求进行翻译。
决定实质等同
器械摘要
Absoanchor Microimplant is the device name listed in this FDA 510(k) record. The listed applicant is Dentos, Inc.. It received FDA 510(k) clearance on 2019-02-05 under 510(k) number K181142. The device is classified under product code OAT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Absoanchor Microimplant?
Absoanchor Microimplant is a medical device that received FDA 510(k) clearance on 2019-02-05. The listed applicant is Dentos, Inc.. The 510(k) number is K181142.
When did Absoanchor Microimplant receive FDA 510(k) clearance?
Absoanchor Microimplant received FDA 510(k) clearance on 2019-02-05, under 510(k) number K181142.
Who is the listed applicant for Absoanchor Microimplant?
The FDA 510(k) record lists Dentos, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Absoanchor Microimplant?
The FDA product code for Absoanchor Microimplant is OAT.
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：OAT）
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。
广告