FDA 510(k)

CryoX 玻璃化冻存试剂盒/解冻试剂盒

K号: K223265 · 2023-05-11

申请人Zhejiang Horizon Medical Technology Co., Ltd.

决定日期2023-05-11

产品代码MQL

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决定实质等同

器械摘要

CryoX Vitrification Freeze Kit / Thaw Kit is the device name listed in this FDA 510(k) record. The listed applicant is Zhejiang Horizon Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-05-11 under 510(k) number K223265. The device is classified under product code MQL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the CryoX Vitrification Freeze Kit / Thaw Kit?

CryoX Vitrification Freeze Kit / Thaw Kit is a medical device that received FDA 510(k) clearance on 2023-05-11. The listed applicant is Zhejiang Horizon Medical Technology Co., Ltd.. The 510(k) number is K223265.

When did CryoX Vitrification Freeze Kit / Thaw Kit receive FDA 510(k) clearance?

CryoX Vitrification Freeze Kit / Thaw Kit received FDA 510(k) clearance on 2023-05-11, under 510(k) number K223265.

Who is the listed applicant for CryoX Vitrification Freeze Kit / Thaw Kit?

The FDA 510(k) record lists Zhejiang Horizon Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CryoX Vitrification Freeze Kit / Thaw Kit?

The FDA product code for CryoX Vitrification Freeze Kit / Thaw Kit is MQL.

列明Zhejiang Horizon Medical Technology Co., Ltd.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。

K232163Lotus单腔卵泡吸管针；Lotus双腔卵泡吸管针

相关器械（代码：MQL）

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。

K254261玻璃化冷冻试剂盒和解冻试剂盒（CS-IVF-FK；CS-IVF-TK）CELL STORE (BEIJING) BIOTECHNOLOGY CO., LTD.K260248超快速升温Kitazato Corporation K252672CaseBio® Culture w/HSA (CMH5)；CaseBio® Handling w/HSA (WHH5)Casebioscience, Inc.K250445Fast Warm - NXFujifilm Irvine Scientific K251637Dewin 生殖培养基（Dewin 精子缓冲液[含HSA和不含HSA]; Dewin 卵泡冲洗液，Dewin 一步法培养基[含HSA和不含HSA]）Donnevie Medical Technology (Shanghai) Co. , Ltd.K251305超快速玻璃化；超快速温控Kitazato Corporation

官方来源

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