Nest VT 液化设备
K号: K233177 · 2024-03-08
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决定日期2024-03-08
产品代码MQK
咨询委员会OB
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器械摘要
Nest VT Vitrification Device is the device name listed in this FDA 510(k) record. The listed applicant is Cook Incorporated. It received FDA 510(k) clearance on 2024-03-08 under 510(k) number K233177. The device is classified under product code MQK. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Nest VT Vitrification Device?
Nest VT Vitrification Device is a medical device that received FDA 510(k) clearance on 2024-03-08. The listed applicant is Cook Incorporated. The 510(k) number is K233177.
When did Nest VT Vitrification Device receive FDA 510(k) clearance?
Nest VT Vitrification Device received FDA 510(k) clearance on 2024-03-08, under 510(k) number K233177.
Who is the listed applicant for Nest VT Vitrification Device?
The FDA 510(k) record lists Cook Incorporated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nest VT Vitrification Device?
The FDA product code for Nest VT Vitrification Device is MQK.
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Cook Incorporated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：MQK）
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。
K241626SperSort™ 精子分离芯片（IPG02）Ipreg IncorporationK241454Minvitro® 玻璃化吸管 (MVT-VSN 系列，包括 MVT-VSNR, MVT-VSNY, MVT-VSNB, MVT-VSNG, MVT-VSNP)Guangzhou Hehong Biotech Co., Ltd.K241348SwimCount® 收割器（1 mL）；SwimCount® 收割器（3 mL）Motilitycount ApsK241341cryo-GO 冷冻玻璃化设备Fujifilm Irvine ScientificK240002G-Vitri™玻璃化吸管Gimbo Medical Technology Shenzhen Co., Ltd.K232980SpermAlign 精子分离装置Cytoswim, Ltd.
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。
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