Capillus 112, Capillus 244
K号: K192012 · 2019-09-12
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申请人Capillus
决定日期2019-09-12
产品代码OAP
咨询委员会PM
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决定实质等同
器械摘要
Capillus 112, Capillus 244 is the device name listed in this FDA 510(k) record. The listed applicant is Capillus. It received FDA 510(k) clearance on 2019-09-12 under 510(k) number K192012. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Capillus 112, Capillus 244?
Capillus 112, Capillus 244 is a medical device that received FDA 510(k) clearance on 2019-09-12. The listed applicant is Capillus. The 510(k) number is K192012.
When did Capillus 112, Capillus 244 receive FDA 510(k) clearance?
Capillus 112, Capillus 244 received FDA 510(k) clearance on 2019-09-12, under 510(k) number K192012.
Who is the listed applicant for Capillus 112, Capillus 244?
The FDA 510(k) record lists Capillus as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Capillus 112, Capillus 244?
The FDA product code for Capillus 112, Capillus 244 is OAP.
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：OAP）
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
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