Pytheas 指导轨迹
K号: K252880 · 2026-05-11
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决定日期2026-05-11
产品代码OLO
咨询委员会NE
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器械摘要
Pytheas Your Guided Trajectory is the device name listed in this FDA 510(k) record. The listed applicant is Pytheas Navigation Sas. It received FDA 510(k) clearance on 2026-05-11 under 510(k) number K252880. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Pytheas Your Guided Trajectory?
Pytheas Your Guided Trajectory is a medical device that received FDA 510(k) clearance on 2026-05-11. The listed applicant is Pytheas Navigation Sas. The 510(k) number is K252880.
When did Pytheas Your Guided Trajectory receive FDA 510(k) clearance?
Pytheas Your Guided Trajectory received FDA 510(k) clearance on 2026-05-11, under 510(k) number K252880.
Who is the listed applicant for Pytheas Your Guided Trajectory?
The FDA 510(k) record lists Pytheas Navigation Sas as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Pytheas Your Guided Trajectory?
The FDA product code for Pytheas Your Guided Trajectory is OLO.
相关临床试验
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相关器械（代码：OLO）
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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