TIA Tip, Cariosity, Transillumination Accessory Tip
K号: K213482 · 2022-04-29
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决定日期2022-04-29
产品代码NTK
咨询委员会DE
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决定实质等同
器械摘要
TIA Tip, Cariosity, Transillumination Accessory Tip is the device name listed in this FDA 510(k) record. The listed applicant is D4D Technologies, LLC. It received FDA 510(k) clearance on 2022-04-29 under 510(k) number K213482. The device is classified under product code NTK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the TIA Tip, Cariosity, Transillumination Accessory Tip?
TIA Tip, Cariosity, Transillumination Accessory Tip is a medical device that received FDA 510(k) clearance on 2022-04-29. The listed applicant is D4D Technologies, LLC. The 510(k) number is K213482.
When did TIA Tip, Cariosity, Transillumination Accessory Tip receive FDA 510(k) clearance?
TIA Tip, Cariosity, Transillumination Accessory Tip received FDA 510(k) clearance on 2022-04-29, under 510(k) number K213482.
Who is the listed applicant for TIA Tip, Cariosity, Transillumination Accessory Tip?
The FDA 510(k) record lists D4D Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TIA Tip, Cariosity, Transillumination Accessory Tip?
The FDA product code for TIA Tip, Cariosity, Transillumination Accessory Tip is NTK.
相关临床试验
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相关器械（代码：NTK）
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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