FESL FINK腔室；FEDL FINK腔室；FETL FINK腔室
K号: K240569 · 2024-11-21
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决定日期2024-11-21
产品代码CBF
咨询委员会AN
请注意，由于您没有提供完整的医疗设备监管文本，我无法提供完整的翻译。如果您能提供完整的文本，我将很乐意为您翻译。
决定实质等同
器械摘要
FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber is the device name listed in this FDA 510(k) record. The listed applicant is Fink Engineering Pty, Ltd.. It received FDA 510(k) clearance on 2024-11-21 under 510(k) number K240569. The device is classified under product code CBF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber?
FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber is a medical device that received FDA 510(k) clearance on 2024-11-21. The listed applicant is Fink Engineering Pty, Ltd.. The 510(k) number is K240569.
When did FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber receive FDA 510(k) clearance?
FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber received FDA 510(k) clearance on 2024-11-21, under 510(k) number K240569.
Who is the listed applicant for FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber?
The FDA 510(k) record lists Fink Engineering Pty, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber?
The FDA product code for FESL FINK Chamber; FEDL FINK Chamber; FETL FINK Chamber is CBF.
相关临床试验
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相关器械（代码：CBF）
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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