AnatomicAligner
K号: K190767 · 2020-03-16
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器械摘要
AnatomicAligner is the device name listed in this FDA 510(k) record. The listed applicant is The Methodist Hospital Research Institute D/B/A Houston. It received FDA 510(k) clearance on 2020-03-16 under 510(k) number K190767. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the AnatomicAligner?
AnatomicAligner is a medical device that received FDA 510(k) clearance on 2020-03-16. The listed applicant is The Methodist Hospital Research Institute D/B/A Houston. The 510(k) number is K190767.
When did AnatomicAligner receive FDA 510(k) clearance?
AnatomicAligner received FDA 510(k) clearance on 2020-03-16, under 510(k) number K190767.
Who is the listed applicant for AnatomicAligner?
The FDA 510(k) record lists The Methodist Hospital Research Institute D/B/A Houston as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AnatomicAligner?
The FDA product code for AnatomicAligner is LLZ.
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相关器械（代码：LLZ）
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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