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K号: K171093 · 2017-07-19
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器械摘要
常见问题
What is the STERILE NITRILE PATIENT EXAMINATION GLOVES, POWDERFREE?
STERILE NITRILE PATIENT EXAMINATION GLOVES, POWDERFREE is a medical device that received FDA 510(k) clearance on 2017-07-19. The listed applicant is Sanrea Healthcare Products Pvt, Ltd.. The 510(k) number is K171093.
When did STERILE NITRILE PATIENT EXAMINATION GLOVES, POWDERFREE receive FDA 510(k) clearance?
STERILE NITRILE PATIENT EXAMINATION GLOVES, POWDERFREE received FDA 510(k) clearance on 2017-07-19, under 510(k) number K171093.
Who is the listed applicant for STERILE NITRILE PATIENT EXAMINATION GLOVES, POWDERFREE?
The FDA 510(k) record lists Sanrea Healthcare Products Pvt, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERILE NITRILE PATIENT EXAMINATION GLOVES, POWDERFREE?
The FDA product code for STERILE NITRILE PATIENT EXAMINATION GLOVES, POWDERFREE 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Sanrea Healthcare Products Pvt, 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: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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