非灭菌无粉乳胶检查手套
K号: K223221 · 2023-01-13
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器械摘要
常见问题
What is the Non-Sterile Powder Free Nitrile Examination Gloves?
Non-Sterile Powder Free Nitrile Examination Gloves is a medical device that received FDA 510(k) clearance on 2023-01-13. The listed applicant is Dynacare Sdn Bhd. The 510(k) number is K223221.
When did Non-Sterile Powder Free Nitrile Examination Gloves receive FDA 510(k) clearance?
Non-Sterile Powder Free Nitrile Examination Gloves received FDA 510(k) clearance on 2023-01-13, under 510(k) number K223221.
Who is the listed applicant for Non-Sterile Powder Free Nitrile Examination Gloves?
The FDA 510(k) record lists Dynacare Sdn Bhd as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Non-Sterile Powder Free Nitrile Examination Gloves?
The FDA product code for Non-Sterile Powder Free Nitrile Examination Gloves 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。
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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