LAITEST 医用口罩
K号: K214035 · 2022-09-13
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决定日期2022-09-13
产品代码FXX
咨询委员会SU
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器械摘要
LAITEST Medical Face Mask is the device name listed in this FDA 510(k) record. The listed applicant is R&R Medical Corporation, Ltd.. It received FDA 510(k) clearance on 2022-09-13 under 510(k) number K214035. The device is classified under product code FXX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the LAITEST Medical Face Mask?
LAITEST Medical Face Mask is a medical device that received FDA 510(k) clearance on 2022-09-13. The listed applicant is R&R Medical Corporation, Ltd.. The 510(k) number is K214035.
When did LAITEST Medical Face Mask receive FDA 510(k) clearance?
LAITEST Medical Face Mask received FDA 510(k) clearance on 2022-09-13, under 510(k) number K214035.
Who is the listed applicant for LAITEST Medical Face Mask?
The FDA 510(k) record lists R&R Medical Corporation, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LAITEST Medical Face Mask?
The FDA product code for LAITEST Medical Face Mask is FXX.
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R&R Medical Corporation, 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：FXX）
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。
K251967HALYARD* FLUIDSHIELD* 3 防雾程序口罩，带有 SO SOFT* 内衬和 SO SOFT* 耳带；HALYARD* FLUIDSHIELD* 3 防雾程序口罩，带有 SO SOFT* 内衬和 SO SOFT* 耳带，带有 WrapAround 护目镜O&M Halyard, Inc.K252534Surgical Face Mask (耳挂式)Zhejiang Hangkang Medical Equipment Co., Ltd.K253398一次性手术口罩（非无菌）(EFX3PLBLKMSK300)Efofex, Inc.K252830一次性外科口罩（3P00B，C2900）Beatles Medical Supplies (Xiantao) Co., Ltd.K252650一次性医用口罩Makrite Industries, Inc.K243342KP防护口罩Kp Trading 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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