Myflon 医用外科口罩 Level 3
K号: K212111 · 2022-01-23
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器械摘要
常见问题
What is the Myflon Surgical Mask Level 3?
Myflon Surgical Mask Level 3 is a medical device that received FDA 510(k) clearance on 2022-01-23. The listed applicant is Feliks Plastik Laminasyon VE Ambalaj Malzemeleri Sanayi. The 510(k) number is K212111.
When did Myflon Surgical Mask Level 3 receive FDA 510(k) clearance?
Myflon Surgical Mask Level 3 received FDA 510(k) clearance on 2022-01-23, under 510(k) number K212111.
Who is the listed applicant for Myflon Surgical Mask Level 3?
The FDA 510(k) record lists Feliks Plastik Laminasyon VE Ambalaj Malzemeleri Sanayi as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Myflon Surgical Mask Level 3?
The FDA product code for Myflon Surgical Mask Level 3 is FXX.
相关临床试验
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列明Feliks Plastik Laminasyon VE Ambalaj Malzemeleri Sanayi为申报人的其他记录
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:FXX)
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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