F65 激光系统
K号: K222790 · 2023-06-14
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决定日期2023-06-14
产品代码OAP
咨询委员会PM
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决定实质等同
器械摘要
F65 Laser System is the device name listed in this FDA 510(k) record. The listed applicant is Lumenis Be, Ltd.. It received FDA 510(k) clearance on 2023-06-14 under 510(k) number K222790. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the F65 Laser System?
F65 Laser System is a medical device that received FDA 510(k) clearance on 2023-06-14. The listed applicant is Lumenis Be, Ltd.. The 510(k) number is K222790.
When did F65 Laser System receive FDA 510(k) clearance?
F65 Laser System received FDA 510(k) clearance on 2023-06-14, under 510(k) number K222790.
Who is the listed applicant for F65 Laser System?
FDA 510(k)记录将Lumenis Be, Ltd.列为申请人。这本身并不能确立该设备的制造商。
What is the FDA product code for F65 Laser System?
The FDA product code for F65 Laser System is OAP.
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Lumenis Be, 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:OAP)
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。
K262183头发生长头盔(TK-176,TK-600,TK-500,TK-282,TK-500A,TK-282A,TK-126,TK-60)Shenzhen Nuon Medical Equipment Co., Ltd.K262254毛发生长梳(X-GC01)Guangdong Ashmore Health Technology Co., Ltd.K261675CHZL红光疗法生发帽(型号:CHZL-120BK-L52D,CHZL-120BK-L53D,CHZL-120BK-L54D)Shenzhen Chuanghong Zhilian Technology Co., Ltd.K261253激光生发设备(HR-H1,HR-H2,HR-H3,HR-H4,HR-H5,HR-H6,HR-H7,HR-H8,HR-H9,HR-H10,HR-I1,HR-I2,HR-I3,HR-I4,HR-I5)Ziree Co., Ltd.K253231激光生发系统(激光帽128,激光头盔272,激光头盔352,激光头盔552,激光头盔500)Hubei Yjt Technology Co.,LtdK260899激光生发设备(F21151,F21152,F21153,F21154,F21155,F21156,F21157,F21158,F21159)Zdeer Technology (Henan) Co., Ltd.
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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