Phantom Trilogy
K号: K213534 · 2022-03-11
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器械摘要
PHantom Trilogy is the device name listed in this FDA 510(k) record. The listed applicant is Resurgeonz, LLC. It received FDA 510(k) clearance on 2022-03-11 under 510(k) number K213534. The device is classified under product code OLI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the PHantom Trilogy?
PHantom Trilogy is a medical device that received FDA 510(k) clearance on 2022-03-11. The listed applicant is Resurgeonz, LLC. The 510(k) number is K213534.
When did PHantom Trilogy receive FDA 510(k) clearance?
PHantom Trilogy received FDA 510(k) clearance on 2022-03-11, under 510(k) number K213534.
Who is the listed applicant for PHantom Trilogy?
The FDA 510(k) record lists Resurgeonz, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PHantom Trilogy?
The FDA product code for PHantom Trilogy is OLI.
相关临床试验
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相关器械（代码：OLI）
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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