Stim2Go
K号: K230701 · 2023-11-24
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决定日期2023-11-24
产品代码IPF
咨询委员会PM
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决定实质等同
器械摘要
Stim2Go is the device name listed in this FDA 510(k) record. The listed applicant is PAJUNK GmbH Medizintechnologie. It received FDA 510(k) clearance on 2023-11-24 under 510(k) number K230701. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Stim2Go?
Stim2Go is a medical device that received FDA 510(k) clearance on 2023-11-24. The listed applicant is PAJUNK GmbH Medizintechnologie. The 510(k) number is K230701.
When did Stim2Go receive FDA 510(k) clearance?
Stim2Go received FDA 510(k) clearance on 2023-11-24, under 510(k) number K230701.
Who is the listed applicant for Stim2Go?
The FDA 510(k) record lists PAJUNK GmbH Medizintechnologie as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Stim2Go?
The FDA product code for Stim2Go is IPF.
列明PAJUNK GmbH Medizintechnologie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。
相关器械（代码：IPF）
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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