CanGaroo RM 抗菌Envelope
K号: K233991 · 2024-06-14
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器械摘要
CanGaroo RM Antibacterial Envelope is the device name listed in this FDA 510(k) record. The listed applicant is Elutia, Inc.. It received FDA 510(k) clearance on 2024-06-14 under 510(k) number K233991. The device is classified under product code FTM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the CanGaroo RM Antibacterial Envelope?
CanGaroo RM Antibacterial Envelope is a medical device that received FDA 510(k) clearance on 2024-06-14. The listed applicant is Elutia, Inc.. The 510(k) number is K233991.
When did CanGaroo RM Antibacterial Envelope receive FDA 510(k) clearance?
CanGaroo RM Antibacterial Envelope received FDA 510(k) clearance on 2024-06-14, under 510(k) number K233991.
Who is the listed applicant for CanGaroo RM Antibacterial Envelope?
The FDA 510(k) record lists Elutia, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CanGaroo RM Antibacterial Envelope?
The FDA product code for CanGaroo RM Antibacterial Envelope is FTM.
相关临床试验
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相关器械（代码：FTM）
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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