免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据,仅供一般参考,不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

天然乳胶无粉检查手套,芦荟

K号: K193150 · 2020-06-05

决定日期2020-06-05
产品代码LZA
咨询委员会医疗设备监管文本翻译如下: HO 请注意,由于您没有提供具体的医疗设备监管文本内容,以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
决定实质等同

器械摘要

Latex Examination Powder Free Glove, Aloe Vera is the device name listed in this FDA 510(k) record. The listed applicant is Top Glove Sdn. Bhd.. It received FDA 510(k) clearance on 2020-06-05 under 510(k) number K193150. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Latex Examination Powder Free Glove, Aloe Vera?

Latex Examination Powder Free Glove, Aloe Vera is a medical device that received FDA 510(k) clearance on 2020-06-05. The listed applicant is Top Glove Sdn. Bhd.. The 510(k) number is K193150.

When did Latex Examination Powder Free Glove, Aloe Vera receive FDA 510(k) clearance?

Latex Examination Powder Free Glove, Aloe Vera received FDA 510(k) clearance on 2020-06-05, under 510(k) number K193150.

Who is the listed applicant for Latex Examination Powder Free Glove, Aloe Vera?

FDA 510(k)记录将Top Glove Sdn. Bhd.列为申请人。这本身并不能确立该设备制造商的身份。

What is the FDA product code for Latex Examination Powder Free Glove, Aloe Vera?

The FDA product code for Latex Examination Powder Free Glove, Aloe Vera 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Top Glove 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。

↑