Explorer Mini
K号: K190682 · 2020-02-27
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申请人Permobil AB
决定日期2020-02-27
产品代码IPL
咨询委员会PM
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决定实质等同
器械摘要
Explorer Mini is the device name listed in this FDA 510(k) record. The listed applicant is Permobil AB. It received FDA 510(k) clearance on 2020-02-27 under 510(k) number K190682. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Explorer Mini?
Explorer Mini is a medical device that received FDA 510(k) clearance on 2020-02-27. The listed applicant is Permobil AB. The 510(k) number is K190682.
When did Explorer Mini receive FDA 510(k) clearance?
Explorer Mini received FDA 510(k) clearance on 2020-02-27, under 510(k) number K190682.
Who is the listed applicant for Explorer Mini?
The FDA 510(k) record lists Permobil AB as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Explorer Mini?
The FDA product code for Explorer Mini is IPL.
相关临床试验
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。
列明Permobil AB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：IPL）
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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