Paragon 成人Maxi PMP 氧合器带管包
K号: K201642 · 2020-09-18
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器械摘要
常见问题
What is the Paragon Adult Maxi PMP Oxygenator with Tubing Pack?
Paragon Adult Maxi PMP Oxygenator with Tubing Pack is a medical device that received FDA 510(k) clearance on 2020-09-18. The listed applicant is Chalice Medical , Ltd.. The 510(k) number is K201642.
When did Paragon Adult Maxi PMP Oxygenator with Tubing Pack receive FDA 510(k) clearance?
Paragon Adult Maxi PMP Oxygenator with Tubing Pack received FDA 510(k) clearance on 2020-09-18, under 510(k) number K201642.
Who is the listed applicant for Paragon Adult Maxi PMP Oxygenator with Tubing Pack?
The FDA 510(k) record lists Chalice Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Paragon Adult Maxi PMP Oxygenator with Tubing Pack?
The FDA product code for Paragon Adult Maxi PMP Oxygenator with Tubing Pack is DTZ.
相关临床试验
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列明Chalice Medical , 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：DTZ）
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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