PIUR tUS inside
K号: K250484 · 2025-06-30
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器械摘要
PIUR tUS inside is the device name listed in this FDA 510(k) record. The listed applicant is Piur Imaging GmbH. It received FDA 510(k) clearance on 2025-06-30 under 510(k) number K250484. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the PIUR tUS inside?
PIUR tUS inside is a medical device that received FDA 510(k) clearance on 2025-06-30. The listed applicant is Piur Imaging GmbH. The 510(k) number is K250484.
When did PIUR tUS inside receive FDA 510(k) clearance?
PIUR tUS inside received FDA 510(k) clearance on 2025-06-30, under 510(k) number K250484.
Who is the listed applicant for PIUR tUS inside?
The FDA 510(k) record lists Piur Imaging GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PIUR tUS inside?
The FDA product code for PIUR tUS inside is QIH.
相关临床试验
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列明Piur Imaging GmbH为申报人的其他记录
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相关器械（代码：QIH）
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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