FDA 510(k)

derma+flex QS 高粘度组织粘合剂

K号: K162352 · 2016-12-22

决定日期2016-12-22

产品代码MPN

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决定实质等同

器械摘要

derma+flex QS High Viscosity Tissue Adhesive is the device name listed in this FDA 510(k) record. The listed applicant is Chemence Medical, Inc.. It received FDA 510(k) clearance on 2016-12-22 under 510(k) number K162352. 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 derma+flex QS High Viscosity Tissue Adhesive?

derma+flex QS High Viscosity Tissue Adhesive is a medical device that received FDA 510(k) clearance on 2016-12-22. The listed applicant is Chemence Medical, Inc.. The 510(k) number is K162352.

When did derma+flex QS High Viscosity Tissue Adhesive receive FDA 510(k) clearance?

derma+flex QS High Viscosity Tissue Adhesive received FDA 510(k) clearance on 2016-12-22, under 510(k) number K162352.

Who is the listed applicant for derma+flex QS High Viscosity Tissue Adhesive?

The FDA 510(k) record lists Chemence Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for derma+flex QS High Viscosity Tissue Adhesive?

The FDA product code for derma+flex QS High Viscosity Tissue Adhesive is MPN.

列明Chemence Medical, Inc.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。

K212246Exofin 精密笔 K200264Exofin 高粘度局部皮肤粘合剂 K191461Exofin 融合皮肤闭合系统 K171442Exofin 融合皮肤闭合系统

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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