Kowa SL-19
K号: K222372 · 2022-11-21
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决定日期2022-11-21
产品代码HJO
咨询委员会OP
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决定实质等同
器械摘要
Kowa SL-19 is the device name listed in this FDA 510(k) record. The listed applicant is Kowa Company , Ltd.. It received FDA 510(k) clearance on 2022-11-21 under 510(k) number K222372. The device is classified under product code HJO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Kowa SL-19?
Kowa SL-19 is a medical device that received FDA 510(k) clearance on 2022-11-21. The listed applicant is Kowa Company , Ltd.. The 510(k) number is K222372.
When did Kowa SL-19 receive FDA 510(k) clearance?
Kowa SL-19 received FDA 510(k) clearance on 2022-11-21, under 510(k) number K222372.
Who is the listed applicant for Kowa SL-19?
The FDA 510(k) record lists Kowa Company , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Kowa SL-19?
The FDA product code for Kowa SL-19 is HJO.
列明Kowa Company , 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：HJO）
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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