医疗设备上抗菌肽涂层的策略：综述与监管科学视角
K号: K220771 · 2022-07-07
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决定日期2022-07-07
产品代码EBI
咨询委员会DE
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决定实质等同
器械摘要
Stratasys TrueDent is the device name listed in this FDA 510(k) record. The listed applicant is Stratasys, Ltd.. It received FDA 510(k) clearance on 2022-07-07 under 510(k) number K220771. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Stratasys TrueDent?
Stratasys TrueDent is a medical device that received FDA 510(k) clearance on 2022-07-07. The listed applicant is Stratasys, Ltd.. The 510(k) number is K220771.
When did Stratasys TrueDent receive FDA 510(k) clearance?
Stratasys TrueDent received FDA 510(k) clearance on 2022-07-07, under 510(k) number K220771.
Who is the listed applicant for Stratasys TrueDent?
The FDA 510(k) record lists Stratasys, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stratasys TrueDent?
The FDA product code for Stratasys TrueDent is EBI.
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：EBI）
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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