PainTB, PainTJ
K号: K203337 · 2022-02-11
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决定日期2022-02-11
产品代码NHN
咨询委员会PM
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决定实质等同
器械摘要
PainTB, PainTJ is the device name listed in this FDA 510(k) record. The listed applicant is Ptech Co., Ltd.. It received FDA 510(k) clearance on 2022-02-11 under 510(k) number K203337. The device is classified under product code NHN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the PainTB, PainTJ?
PainTB, PainTJ is a medical device that received FDA 510(k) clearance on 2022-02-11. The listed applicant is Ptech Co., Ltd.. The 510(k) number is K203337.
When did PainTB, PainTJ receive FDA 510(k) clearance?
PainTB, PainTJ received FDA 510(k) clearance on 2022-02-11, under 510(k) number K203337.
Who is the listed applicant for PainTB, PainTJ?
The FDA 510(k) record lists Ptech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PainTB, PainTJ?
The FDA product code for PainTB, PainTJ is NHN.
相关临床试验
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相关器械（代码：NHN）
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
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