FDA 510(k)

V-SPERM 清洗器

K号: K223117 · 2023-01-31

决定日期2023-01-31

产品代码MQL

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决定实质等同

器械摘要

V-SPERM WASH is the device name listed in this FDA 510(k) record. The listed applicant is Vitromed GmbH. It received FDA 510(k) clearance on 2023-01-31 under 510(k) number K223117. 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 V-SPERM WASH?

V-SPERM WASH is a medical device that received FDA 510(k) clearance on 2023-01-31. The listed applicant is Vitromed GmbH. The 510(k) number is K223117.

When did V-SPERM WASH receive FDA 510(k) clearance?

V-SPERM WASH received FDA 510(k) clearance on 2023-01-31, under 510(k) number K223117.

Who is the listed applicant for V-SPERM WASH?

The FDA 510(k) record lists Vitromed GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for V-SPERM WASH?

The FDA product code for V-SPERM WASH is MQL.

列明Vitromed GmbH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。

K241833V-GRAD K240176V-VITFREEZE 和 V-VITWARM K232125V-PVP K222606V-HYADASE K193285V-单步 K192146V-DENUPET

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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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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。