Lascod 印模材料
K号: K201184 · 2020-05-05
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申请人Lascod Spa
决定日期2020-05-05
产品代码ELW
咨询委员会DE
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决定实质等同
器械摘要
Lascod Impression Materials is the device name listed in this FDA 510(k) record. The listed applicant is Lascod Spa. It received FDA 510(k) clearance on 2020-05-05 under 510(k) number K201184. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Lascod Impression Materials?
Lascod Impression Materials is a medical device that received FDA 510(k) clearance on 2020-05-05. The listed applicant is Lascod Spa. The 510(k) number is K201184.
When did Lascod Impression Materials receive FDA 510(k) clearance?
Lascod Impression Materials received FDA 510(k) clearance on 2020-05-05, under 510(k) number K201184.
Who is the listed applicant for Lascod Impression Materials?
The FDA 510(k) record lists Lascod Spa as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Lascod Impression Materials?
The FDA product code for Lascod Impression Materials is ELW.
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：ELW）
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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