Welch Allyn Connex® 360（多款）
K号: K243598 · 2025-07-13
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器械摘要
Welch Allyn Connex® 360 (Multiple) is the device name listed in this FDA 510(k) record. The listed applicant is Welch Allyn, Inc.. It received FDA 510(k) clearance on 2025-07-13 under 510(k) number K243598. FDA Decision: Substantially Equivalent.
常见问题
What is the Welch Allyn Connex® 360 (Multiple)?
Welch Allyn Connex® 360 (Multiple) is a medical device that received FDA 510(k) clearance on 2025-07-13. The listed applicant is Welch Allyn, Inc.. The 510(k) number is K243598.
When did Welch Allyn Connex® 360 (Multiple) receive FDA 510(k) clearance?
Welch Allyn Connex® 360 (Multiple) received FDA 510(k) clearance on 2025-07-13, under 510(k) number K243598.
Who is the listed applicant for Welch Allyn Connex® 360 (Multiple)?
The FDA 510(k) record lists Welch Allyn, Inc. as the applicant. This does not by itself establish the device manufacturer.
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Welch Allyn, Inc.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。
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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