F&P 850 AirSpiral成人NIV和NHF电路套件
K号: K212031 · 2022-04-22
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器械摘要
常见问题
What is the F&P 850 AirSpiral Adult NIV and NHF Circuit Kit?
F&P 850 AirSpiral Adult NIV and NHF Circuit Kit is a medical device that received FDA 510(k) clearance on 2022-04-22. The listed applicant is Fisher & Paykel Healthcare, Ltd.. The 510(k) number is K212031.
When did F&P 850 AirSpiral Adult NIV and NHF Circuit Kit receive FDA 510(k) clearance?
F&P 850 AirSpiral Adult NIV and NHF Circuit Kit received FDA 510(k) clearance on 2022-04-22, under 510(k) number K212031.
Who is the listed applicant for F&P 850 AirSpiral Adult NIV and NHF Circuit Kit?
The FDA 510(k) record lists Fisher & Paykel Healthcare, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for F&P 850 AirSpiral Adult NIV and NHF Circuit Kit?
The FDA product code for F&P 850 AirSpiral Adult NIV and NHF Circuit Kit is BTT.
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Fisher & Paykel Healthcare, 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：BTT）
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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