NeoSculpt Plus
K号: K252888 · 2026-03-09
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决定日期2026-03-09
产品代码PBX
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
NeoSculpt Plus is the device name listed in this FDA 510(k) record. The listed applicant is S&M Medical Co., Ltd.. It received FDA 510(k) clearance on 2026-03-09 under 510(k) number K252888. The device is classified under product code PBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the NeoSculpt Plus?
NeoSculpt Plus is a medical device that received FDA 510(k) clearance on 2026-03-09. The listed applicant is S&M Medical Co., Ltd.. The 510(k) number is K252888.
When did NeoSculpt Plus receive FDA 510(k) clearance?
NeoSculpt Plus received FDA 510(k) clearance on 2026-03-09, under 510(k) number K252888.
Who is the listed applicant for NeoSculpt Plus?
The FDA 510(k) record lists S&M Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NeoSculpt Plus?
The FDA product code for NeoSculpt Plus is PBX.
相关临床试验
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相关器械（代码：PBX）
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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