泰坦银 200
K号: K173844 · 2018-08-09
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器械摘要
Titan Ag 200 is the device name listed in this FDA 510(k) record. The listed applicant is Specialty Fibres and Materials, Ltd.. It received FDA 510(k) clearance on 2018-08-09 under 510(k) number K173844. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.
常见问题
What is the Titan Ag 200?
Titan Ag 200 is a medical device that received FDA 510(k) clearance on 2018-08-09. The listed applicant is Specialty Fibres and Materials, Ltd.. The 510(k) number is K173844.
When did Titan Ag 200 receive FDA 510(k) clearance?
Titan Ag 200 received FDA 510(k) clearance on 2018-08-09, under 510(k) number K173844.
Who is the listed applicant for Titan Ag 200?
The FDA 510(k) record lists Specialty Fibres and Materials, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Titan Ag 200?
The FDA product code for Titan Ag 200 is FRO. This falls under the Anesthesiology category.
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：FRO）
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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