SurgiLance® Safety Lancet
K号: K222224 · 2022-09-22
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决定日期2022-09-22
产品代码FMK
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
决定实质等同
器械摘要
SurgiLance® Safety Lancet is the device name listed in this FDA 510(k) record. The listed applicant is Medipurpose Pte. , Ltd.. It received FDA 510(k) clearance on 2022-09-22 under 510(k) number K222224. The device is classified under product code FMK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the SurgiLance® Safety Lancet?
SurgiLance® Safety Lancet is a medical device that received FDA 510(k) clearance on 2022-09-22. The listed applicant is Medipurpose Pte. , Ltd.. The 510(k) number is K222224.
When did SurgiLance® Safety Lancet receive FDA 510(k) clearance?
SurgiLance® Safety Lancet received FDA 510(k) clearance on 2022-09-22, under 510(k) number K222224.
Who is the listed applicant for SurgiLance® Safety Lancet?
The FDA 510(k) record lists Medipurpose Pte. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SurgiLance® Safety Lancet?
The FDA product code for SurgiLance® Safety Lancet is FMK.
相关临床试验
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相关器械（代码：FMK）
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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