Synchrony (20-3000)
K号: K242704 · 2025-06-05
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决定日期2025-06-05
产品代码GZI
咨询委员会NE
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决定实质等同
器械摘要
Synchrony (20-3000) is the device name listed in this FDA 510(k) record. The listed applicant is Synapse Biomedical, Inc.. It received FDA 510(k) clearance on 2025-06-05 under 510(k) number K242704. The device is classified under product code GZI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Synchrony (20-3000)?
Synchrony (20-3000) is a medical device that received FDA 510(k) clearance on 2025-06-05. The listed applicant is Synapse Biomedical, Inc.. The 510(k) number is K242704.
When did Synchrony (20-3000) receive FDA 510(k) clearance?
Synchrony (20-3000) received FDA 510(k) clearance on 2025-06-05, under 510(k) number K242704.
Who is the listed applicant for Synchrony (20-3000)?
The FDA 510(k) record lists Synapse Biomedical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Synchrony (20-3000)?
The FDA product code for Synchrony (20-3000) is GZI.
相关临床试验
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相关器械（代码：GZI）
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。
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