Terran NM-101
K号: K230187 · 2023-09-29
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器械摘要
Terran NM-101 is the device name listed in this FDA 510(k) record. The listed applicant is Terran Biosciences, Inc.. It received FDA 510(k) clearance on 2023-09-29 under 510(k) number K230187. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Terran NM-101?
Terran NM-101 is a medical device that received FDA 510(k) clearance on 2023-09-29. The listed applicant is Terran Biosciences, Inc.. The 510(k) number is K230187.
When did Terran NM-101 receive FDA 510(k) clearance?
Terran NM-101 received FDA 510(k) clearance on 2023-09-29, under 510(k) number K230187.
Who is the listed applicant for Terran NM-101?
The FDA 510(k) record lists Terran Biosciences, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Terran NM-101?
The FDA product code for Terran NM-101 is LNH.
相关临床试验
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相关器械（代码：LNH）
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
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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