Cliq 吸引器
K号: K201203 · 2020-09-03
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决定日期2020-09-03
产品代码BTA
咨询委员会SU
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决定实质等同
器械摘要
Cliq Aspirator is the device name listed in this FDA 510(k) record. The listed applicant is Anest Iwata Sparmax Co., Ltd.. It received FDA 510(k) clearance on 2020-09-03 under 510(k) number K201203. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Cliq Aspirator?
Cliq Aspirator is a medical device that received FDA 510(k) clearance on 2020-09-03. The listed applicant is Anest Iwata Sparmax Co., Ltd.. The 510(k) number is K201203.
When did Cliq Aspirator receive FDA 510(k) clearance?
Cliq Aspirator received FDA 510(k) clearance on 2020-09-03, under 510(k) number K201203.
Who is the listed applicant for Cliq Aspirator?
The FDA 510(k) record lists Anest Iwata Sparmax Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Cliq Aspirator?
The FDA product code for Cliq Aspirator is BTA.
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：BTA）
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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