蓝色无粉患者检查手套,非无菌
K号: K220431 · 2022-06-17
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器械摘要
常见问题
What is the Blue Nitrile Powder-Free Patient Examination Glove, Non-Sterile?
Blue Nitrile Powder-Free Patient Examination Glove, Non-Sterile is a medical device that received FDA 510(k) clearance on 2022-06-17. The listed applicant is One Glove Industrial Sdn Bhd. The 510(k) number is K220431.
When did Blue Nitrile Powder-Free Patient Examination Glove, Non-Sterile receive FDA 510(k) clearance?
Blue Nitrile Powder-Free Patient Examination Glove, Non-Sterile received FDA 510(k) clearance on 2022-06-17, under 510(k) number K220431.
Who is the listed applicant for Blue Nitrile Powder-Free Patient Examination Glove, Non-Sterile?
The FDA 510(k) record lists One Glove Industrial Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Blue Nitrile Powder-Free Patient Examination Glove, Non-Sterile?
The FDA product code for Blue Nitrile Powder-Free Patient Examination Glove, Non-Sterile is LZA.
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One Glove Industrial Sdn Bhd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:LZA)
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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