RELI REDIDIOX 染色,RELI REDIDIOX,RELI REDIDIOX 未染色
K号: K161737 · 2017-03-02
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器械摘要
常见问题
What is the RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed?
RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed is a medical device that received FDA 510(k) clearance on 2017-03-02. The listed applicant is Myco Medical. The 510(k) number is K161737.
When did RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed receive FDA 510(k) clearance?
RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed received FDA 510(k) clearance on 2017-03-02, under 510(k) number K161737.
Who is the listed applicant for RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed?
The FDA 510(k) record lists Myco Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed?
The FDA product code for RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX Undyed is NEW.
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:NEW)
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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