FDA 510(k)

LiquiBand Plus

K号: K183570 · 2020-03-09

决定日期2020-03-09

产品代码MPN

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决定实质等同

器械摘要

LiquiBand Plus is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Medical Solutions Limited. It received FDA 510(k) clearance on 2020-03-09 under 510(k) number K183570. The device is classified under product code MPN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the LiquiBand Plus?

LiquiBand Plus is a medical device that received FDA 510(k) clearance on 2020-03-09. The listed applicant is Advanced Medical Solutions Limited. The 510(k) number is K183570.

When did LiquiBand Plus receive FDA 510(k) clearance?

LiquiBand Plus received FDA 510(k) clearance on 2020-03-09, under 510(k) number K183570.

Who is the listed applicant for LiquiBand Plus?

The FDA 510(k) record lists Advanced Medical Solutions Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LiquiBand Plus?

The FDA product code for LiquiBand Plus is MPN.

列明Advanced Medical Solutions Limited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。

K223310含PHMB的抗菌硅胶泡沫伤口敷料 K211878LiquiBand XL

相关器械（代码：MPN）

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。

K243990BondEase 2 表面皮肤粘合剂Optmed, Inc.K250950CUTIVA™局部皮肤粘合剂（RM1700）；CUTIVA™ PLUS皮肤闭合系统（RM1739）Okapi Medical, LLC Dba Resivant Medical K234114CUTIVA™局部皮肤粘合剂（RM-1700）；CUTIVA™ PLUS皮肤闭合系统（RM-1739）Okapi Medical, LLC Dba Resivant Medical K233458CM005 标准 (CM005)；CM004 迷你 (CM004)Connexicon Medical , Ltd.K230981Meriglu局部皮肤粘合剂M/s. Meril Endo Surgery Private Limited.K212246Exofin 精密笔Chemence Medical, Inc.

官方来源

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