mi-eye 3 带导管内窥镜,mi-tablet 3
K号: K212556 · 2021-09-15
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器械摘要
常见问题
What is the mi-eye 3 needlescope with cannula, mi-tablet 3?
mi-eye 3 needlescope with cannula, mi-tablet 3 is a medical device that received FDA 510(k) clearance on 2021-09-15. The listed applicant is Trice Medical, Inc.. The 510(k) number is K212556.
When did mi-eye 3 needlescope with cannula, mi-tablet 3 receive FDA 510(k) clearance?
mi-eye 3 needlescope with cannula, mi-tablet 3 received FDA 510(k) clearance on 2021-09-15, under 510(k) number K212556.
Who is the listed applicant for mi-eye 3 needlescope with cannula, mi-tablet 3?
The FDA 510(k) record lists Trice Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for mi-eye 3 needlescope with cannula, mi-tablet 3?
The FDA product code for mi-eye 3 needlescope with cannula, mi-tablet 3 is HRX.
相关临床试验
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列明Trice Medical, Inc.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:HRX)
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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