免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据,仅供一般参考,不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

Ultra RapidWarm™ Blast

K号: K240605 · 2024-08-07

决定日期2024-08-07
产品代码MQL
咨询委员会OB 请注意,由于您没有提供具体的医疗设备监管文本,我无法进行翻译。请提供具体的文本内容,以便我能够按照您的要求进行翻译。
决定实质等同

器械摘要

Ultra RapidWarm™ Blast is the device name listed in this FDA 510(k) record. The listed applicant is Vitrolife Sweden AB. It received FDA 510(k) clearance on 2024-08-07 under 510(k) number K240605. 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 Ultra RapidWarm™ Blast?

Ultra RapidWarm™ Blast is a medical device that received FDA 510(k) clearance on 2024-08-07. The listed applicant is Vitrolife Sweden AB. The 510(k) number is K240605.

When did Ultra RapidWarm™ Blast receive FDA 510(k) clearance?

Ultra RapidWarm™ Blast received FDA 510(k) clearance on 2024-08-07, under 510(k) number K240605.

Who is the listed applicant for Ultra RapidWarm™ Blast?

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

What is the FDA product code for Ultra RapidWarm™ Blast?

The FDA product code for Ultra RapidWarm™ Blast is MQL.

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Vitrolife Sweden AB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。

查看所有 8 个设备 →

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。

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。

↑