Panther TPS
K号: K231825 · 2023-12-15
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器械摘要
Panther TPS is the device name listed in this FDA 510(k) record. The listed applicant is Prowess, Inc.. It received FDA 510(k) clearance on 2023-12-15 under 510(k) number K231825. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Panther TPS?
Panther TPS is a medical device that received FDA 510(k) clearance on 2023-12-15. The listed applicant is Prowess, Inc.. The 510(k) number is K231825.
When did Panther TPS receive FDA 510(k) clearance?
Panther TPS received FDA 510(k) clearance on 2023-12-15, under 510(k) number K231825.
Who is the listed applicant for Panther TPS?
The FDA 510(k) record lists Prowess, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Panther TPS?
The FDA product code for Panther TPS is MUJ.
相关临床试验
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列明Prowess, Inc.为申报人的其他记录
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相关器械（代码：MUJ）
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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