UNiD脊柱分析仪
K号: K212005 · 2022-01-12
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器械摘要
UNiD Spine Analyzer is the device name listed in this FDA 510(k) record. The listed applicant is Medicrea International, Inc.. It received FDA 510(k) clearance on 2022-01-12 under 510(k) number K212005. 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 UNiD Spine Analyzer?
UNiD Spine Analyzer is a medical device that received FDA 510(k) clearance on 2022-01-12. The listed applicant is Medicrea International, Inc.. The 510(k) number is K212005.
When did UNiD Spine Analyzer receive FDA 510(k) clearance?
UNiD Spine Analyzer received FDA 510(k) clearance on 2022-01-12, under 510(k) number K212005.
Who is the listed applicant for UNiD Spine Analyzer?
The FDA 510(k) record lists Medicrea International, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UNiD Spine Analyzer?
The FDA product code for UNiD Spine Analyzer is LLZ.
相关临床试验
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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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