FDA 510(k)

Biogel Skinsense 指示性手套，Biogel PI Ultratouch，Biogel PI 指示性手套，Biogel PI，Biogel PI Micro

K号: K193573 · 2020-04-10

决定日期2020-04-10

产品代码KGO

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决定实质等同

器械摘要

Biogel Skinsense Indicator Underglove, Biogel PI Ultratouch, Biogel PI Indicator Underglove, Biogel PI, Biogel PI Micro is the device name listed in this FDA 510(k) record. The listed applicant is Molnlycke Health Care Us, LLC. It received FDA 510(k) clearance on 2020-04-10 under 510(k) number K193573. 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 Biogel Skinsense Indicator Underglove, Biogel PI Ultratouch, Biogel PI Indicator Underglove, Biogel PI, Biogel PI Micro?

Biogel Skinsense Indicator Underglove, Biogel PI Ultratouch, Biogel PI Indicator Underglove, Biogel PI, Biogel PI Micro is a medical device that received FDA 510(k) clearance on 2020-04-10. The listed applicant is Molnlycke Health Care Us, LLC. The 510(k) number is K193573.

When did Biogel Skinsense Indicator Underglove, Biogel PI Ultratouch, Biogel PI Indicator Underglove, Biogel PI, Biogel PI Micro receive FDA 510(k) clearance?

Biogel Skinsense Indicator Underglove, Biogel PI Ultratouch, Biogel PI Indicator Underglove, Biogel PI, Biogel PI Micro received FDA 510(k) clearance on 2020-04-10, under 510(k) number K193573.

Who is the listed applicant for Biogel Skinsense Indicator Underglove, Biogel PI Ultratouch, Biogel PI Indicator Underglove, Biogel PI, Biogel PI Micro?

The FDA 510(k) record lists Molnlycke Health Care Us, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Biogel Skinsense Indicator Underglove, Biogel PI Ultratouch, Biogel PI Indicator Underglove, Biogel PI, Biogel PI Micro?

The FDA product code for Biogel Skinsense Indicator Underglove, Biogel PI Ultratouch, Biogel PI Indicator Underglove, Biogel PI, Biogel PI Micro is KGO.

列明Molnlycke Health Care Us, LLC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。

K232508Barrier EasyWarm 活性自加热毯 K203369Avance单负压伤口治疗（NPWT）系统 K202090Biogel Eclipse / Biogel Eclipse 指示性手套，Biogel 外科医生 / Biogel 指示性手套，Biogel PI 微型指示性手套，Biogel PI UltraTouch S 外科手套具有低皮炎潜力声明，Biogel PI UltraTouch S 指示性手套具有低皮炎潜力声明 K191869Biogel(R) PI UltraTouch S 外科手套具有低皮炎潜力声明，Biogel(R) PI UltraTouch S 指示性手套具有低皮炎潜力声明 K190077Biogel® PI UltraTouch S 外科手套，Biogel® Pl Ultra Touch S 指示性手套 K161939Avance腹部敷料套装

查看所有 12 个设备 →

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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