压缩治疗设备型号LGT-2200SP
K号: K191862 · 2019-10-29
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器械摘要
常见问题
What is the Compression Therapy Device Model LGT-2200SP?
Compression Therapy Device Model LGT-2200SP is a medical device that received FDA 510(k) clearance on 2019-10-29. The listed applicant is Guangzhou Longest Science & Technology Co., Ltd.. The 510(k) number is K191862.
When did Compression Therapy Device Model LGT-2200SP receive FDA 510(k) clearance?
Compression Therapy Device Model LGT-2200SP received FDA 510(k) clearance on 2019-10-29, under 510(k) number K191862.
Who is the listed applicant for Compression Therapy Device Model LGT-2200SP?
The FDA 510(k) record lists Guangzhou Longest Science & Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Compression Therapy Device Model LGT-2200SP?
The FDA product code for Compression Therapy Device Model LGT-2200SP is IRP.
相关临床试验
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列明Guangzhou Longest Science & Technology Co., Ltd.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：IRP）
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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