OncoStudio
K号: K260528 · 2026-07-02
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器械摘要
OncoStudio is the device name listed in this FDA 510(k) record. The listed applicant is Oncosoft. Inc.,. It received FDA 510(k) clearance on 2026-07-02 under 510(k) number K260528. The device is classified under product code QKB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the OncoStudio?
OncoStudio is a medical device that received FDA 510(k) clearance on 2026-07-02. The listed applicant is Oncosoft. Inc.,. The 510(k) number is K260528.
When did OncoStudio receive FDA 510(k) clearance?
OncoStudio received FDA 510(k) clearance on 2026-07-02, under 510(k) number K260528.
Who is the listed applicant for OncoStudio?
The FDA 510(k) record lists Oncosoft. Inc., as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OncoStudio?
The FDA product code for OncoStudio is QKB.
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相关器械（代码：QKB）
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
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