VMAT PRO
K号: K243488 · 2025-02-06
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申请人Termosalud
决定日期2025-02-06
产品代码ISA
咨询委员会PM
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决定实质等同
器械摘要
VMAT PRO is the device name listed in this FDA 510(k) record. The listed applicant is Termosalud. It received FDA 510(k) clearance on 2025-02-06 under 510(k) number K243488. The device is classified under product code ISA. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the VMAT PRO?
VMAT PRO is a medical device that received FDA 510(k) clearance on 2025-02-06. The listed applicant is Termosalud. The 510(k) number is K243488.
When did VMAT PRO receive FDA 510(k) clearance?
VMAT PRO received FDA 510(k) clearance on 2025-02-06, under 510(k) number K243488.
Who is the listed applicant for VMAT PRO?
The FDA 510(k) record lists Termosalud as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VMAT PRO?
The FDA product code for VMAT PRO is ISA.
列明Termosalud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：ISA）
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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