Brightway品牌乳胶检查手套,无粉(薰衣草)
K号: K162146 · 2017-01-05
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器械摘要
常见问题
What is the Brightway Brand Nitrile Examination Gloves, Powder Free (Lavender)?
Brightway Brand Nitrile Examination Gloves, Powder Free (Lavender) is a medical device that received FDA 510(k) clearance on 2017-01-05. The listed applicant is Brightway Holdings Sdn. Bhd.. The 510(k) number is K162146.
When did Brightway Brand Nitrile Examination Gloves, Powder Free (Lavender) receive FDA 510(k) clearance?
Brightway Brand Nitrile Examination Gloves, Powder Free (Lavender) received FDA 510(k) clearance on 2017-01-05, under 510(k) number K162146.
Who is the listed applicant for Brightway Brand Nitrile Examination Gloves, Powder Free (Lavender)?
The FDA 510(k) record lists Brightway Holdings Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Brightway Brand Nitrile Examination Gloves, Powder Free (Lavender)?
The FDA product code for Brightway Brand Nitrile Examination Gloves, Powder Free (Lavender) 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Brightway Holdings 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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