组织态
K号: K231277 · 2023-11-09
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器械摘要
TissueStat is the device name listed in this FDA 510(k) record. The listed applicant is Durastat, LLC. It received FDA 510(k) clearance on 2023-11-09 under 510(k) number K231277. The device is classified under product code NBY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the TissueStat?
TissueStat is a medical device that received FDA 510(k) clearance on 2023-11-09. The listed applicant is Durastat, LLC. The 510(k) number is K231277.
When did TissueStat receive FDA 510(k) clearance?
TissueStat received FDA 510(k) clearance on 2023-11-09, under 510(k) number K231277.
Who is the listed applicant for TissueStat?
The FDA 510(k) record lists Durastat, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TissueStat?
The FDA product code for TissueStat is NBY.
相关临床试验
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相关器械（代码：NBY）
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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