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FDA 510(k)

EasiSlush® 生理盐水溶液,用于无菌冰冻混合物制备 (BTLE-1250)

K号: K243618 · 2025-06-17

决定日期2025-06-17
产品代码KDN
咨询委员会GU 请注意,由于您只提供了“GU”这个词,我无法提供完整的翻译。如果您能提供完整的句子或段落,我将能够为您提供准确的翻译。
决定实质等同

器械摘要

EasiSlush® Sodium Chloride Solution for Sterile Slush Preparation (BTLE-1250) is the device name listed in this FDA 510(k) record. The listed applicant is Bridge TO Life. It received FDA 510(k) clearance on 2025-06-17 under 510(k) number K243618. The device is classified under product code KDN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the EasiSlush® Sodium Chloride Solution for Sterile Slush Preparation (BTLE-1250)?

EasiSlush® Sodium Chloride Solution for Sterile Slush Preparation (BTLE-1250) is a medical device that received FDA 510(k) clearance on 2025-06-17. The listed applicant is Bridge TO Life. The 510(k) number is K243618.

When did EasiSlush® Sodium Chloride Solution for Sterile Slush Preparation (BTLE-1250) receive FDA 510(k) clearance?

EasiSlush® Sodium Chloride Solution for Sterile Slush Preparation (BTLE-1250) received FDA 510(k) clearance on 2025-06-17, under 510(k) number K243618.

Who is the listed applicant for EasiSlush® Sodium Chloride Solution for Sterile Slush Preparation (BTLE-1250)?

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

What is the FDA product code for EasiSlush® Sodium Chloride Solution for Sterile Slush Preparation (BTLE-1250)?

The FDA product code for EasiSlush® Sodium Chloride Solution for Sterile Slush Preparation (BTLE-1250) is KDN.

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Bridge TO Life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:KDN)

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

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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。

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