SLIMUS
K号: K192970 · 2020-12-01
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器械摘要
SLIMUS is the device name listed in this FDA 510(k) record. The listed applicant is Hironic Co., Ltd.. It received FDA 510(k) clearance on 2020-12-01 under 510(k) number K192970. The device is classified under product code PKT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the SLIMUS?
SLIMUS is a medical device that received FDA 510(k) clearance on 2020-12-01. The listed applicant is Hironic Co., Ltd.. The 510(k) number is K192970.
When did SLIMUS receive FDA 510(k) clearance?
SLIMUS received FDA 510(k) clearance on 2020-12-01, under 510(k) number K192970.
Who is the listed applicant for SLIMUS?
FDA 510(k)记录将Hironic Co., Ltd.列为申请人。这本身并不能确立该设备制造商的身份。
What is the FDA product code for SLIMUS?
The FDA product code for SLIMUS is PKT.
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。
列明Hironic Co., Ltd.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：PKT）
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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