验证蒸汽集成指示器
K号: K243876 · 2025-04-25
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决定日期2025-04-25
产品代码JOJ
咨询委员会医疗设备监管文本翻译如下：
HO
请注意，由于您没有提供具体的医疗设备监管文本内容，以上仅为示例。请提供具体的文本内容以便进行准确的翻译。
决定实质等同
器械摘要
VERIFY STEAM Integrating Indicator is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2025-04-25 under 510(k) number K243876. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the VERIFY STEAM Integrating Indicator?
VERIFY STEAM Integrating Indicator is a medical device that received FDA 510(k) clearance on 2025-04-25. The listed applicant is STERIS Corporation. The 510(k) number is K243876.
When did VERIFY STEAM Integrating Indicator receive FDA 510(k) clearance?
VERIFY STEAM Integrating Indicator received FDA 510(k) clearance on 2025-04-25, under 510(k) number K243876.
Who is the listed applicant for VERIFY STEAM Integrating Indicator?
The FDA 510(k) record lists STERIS Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VERIFY STEAM Integrating Indicator?
The FDA product code for VERIFY STEAM Integrating Indicator is JOJ.
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STERIS Corporation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：JOJ）
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。
K2619923M™ Attest™ 蒸汽化学集成器（1243A、1243B、1243RE、1243RES）Solventum US, LLCK260181LF 蒸汽灭菌过程指示胶带Intertape Polymer GroupK251991SafeSecure 蒸汽灭菌过程指示器（4012，4013，4014，4016）；SafeSecure 氢氧化过氧化物蒸汽灭菌过程指示器（4211，4212，4213）Shenzhen Safesecure Medical Infection Control Tech Co. , Ltd.K251035DISINTEK™ PA 测试条Serim ResearchK251048Rapicide PA 高级消毒测试条 模型参考号 = ML02-0118STERIS CorporationK250172Green Card Bowie-Dick Test (BD115)Steritec Products, Inc. (A Getinge Company)
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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