再处理超级扭矩和超级扭矩加诊断血管造影导管
K号: K231015 · 2024-07-01
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器械摘要
常见问题
What is the Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters?
Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters is a medical device that received FDA 510(k) clearance on 2024-07-01. The listed applicant is Innovative Health, LLC. The 510(k) number is K231015.
When did Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters receive FDA 510(k) clearance?
Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters received FDA 510(k) clearance on 2024-07-01, under 510(k) number K231015.
Who is the listed applicant for Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters?
The FDA 510(k) record lists Innovative Health, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters?
The FDA product code for Reprocessed Super Torque and Super Torque Plus Diagnostic Angiographic Catheters is NLI.
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列明Innovative Health, LLC为申报人的其他记录
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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