FDA 510(k)

无菌无粉乳胶外科手套

K号: K221424 · 2023-01-26

决定日期2023-01-26

产品代码KGO

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决定实质等同

器械摘要

Sterile Surgical Powder Free Latex Glove is the device name listed in this FDA 510(k) record. The listed applicant is New Era Medicare Sdn. Bhd.. It received FDA 510(k) clearance on 2023-01-26 under 510(k) number K221424. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Sterile Surgical Powder Free Latex Glove?

Sterile Surgical Powder Free Latex Glove is a medical device that received FDA 510(k) clearance on 2023-01-26. The listed applicant is New Era Medicare Sdn. Bhd.. The 510(k) number is K221424.

When did Sterile Surgical Powder Free Latex Glove receive FDA 510(k) clearance?

Sterile Surgical Powder Free Latex Glove received FDA 510(k) clearance on 2023-01-26, under 510(k) number K221424.

Who is the listed applicant for Sterile Surgical Powder Free Latex Glove?

The FDA 510(k) record lists New Era Medicare Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sterile Surgical Powder Free Latex Glove?

The FDA product code for Sterile Surgical Powder Free Latex Glove is KGO.

列明New Era Medicare 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。

K230314无菌粉无乳胶检查手套（蓝色、黑色和白色）K221667非无菌无粉乳胶检查手套

相关器械（代码：KGO）

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。

K260558无粉乳胶外科手套，适用于化疗药物和芬太尼盐酸盐的使用测试；含胶体燕麦的无粉乳胶外科手套，适用于化疗药物和芬太尼盐酸盐的使用测试Hartalega NGC Sdn. Bhd.K253060无菌乳胶无粉手术手套Protect Gloves Company Limited K250313无菌无粉合成橡胶外科手套，绿色，经测试可用于化疗药物和胃酸Harps Europe Manufacturing GmbH K240790聚异戊二烯手术手套Suzhou Colour-Way New Material Co., Ltd.K232079天然橡胶乳胶外科手套，无粉，无菌，经化疗药物和芬太尼使用测试（绿色）；天然橡胶乳胶（条状/涂层）/（条状/包装）外科手套，无粉，无菌，经化疗药物和芬太尼使用测试Wrp Asia Pacific Sdn. Bhd.K232444无菌粉无乳胶手术手套，用于化疗药物测试Grand Work Plastic Products Co., Ltd.

官方来源

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