LF 蒸汽灭菌过程指示胶带
K号: K260181 · 2026-02-20
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决定日期2026-02-20
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
LF Process Indicator Tape for Steam Sterilization is the device name listed in this FDA 510(k) record. The listed applicant is Intertape Polymer Group. It received FDA 510(k) clearance on 2026-02-20 under 510(k) number K260181. 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 LF Process Indicator Tape for Steam Sterilization?
LF Process Indicator Tape for Steam Sterilization is a medical device that received FDA 510(k) clearance on 2026-02-20. The listed applicant is Intertape Polymer Group. The 510(k) number is K260181.
When did LF Process Indicator Tape for Steam Sterilization receive FDA 510(k) clearance?
LF Process Indicator Tape for Steam Sterilization received FDA 510(k) clearance on 2026-02-20, under 510(k) number K260181.
Who is the listed applicant for LF Process Indicator Tape for Steam Sterilization?
The FDA 510(k) record lists Intertape Polymer Group as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LF Process Indicator Tape for Steam Sterilization?
The FDA product code for LF Process Indicator Tape for Steam Sterilization 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。
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, LLCK251991SafeSecure 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 CorporationK243876验证蒸汽集成指示器STERIS 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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