FDA 510(k)

STERRAD® 100NX 消毒器，配备 ALLClear® 技术（10104）

K号: K250802 · 2025-04-14

申请人Advanced Sterilization Products, Inc.

决定日期2025-04-14

产品代码MLR

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

STERRAD® 100NX Sterilizer with ALLClear™ Technology (10104) is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Sterilization Products, Inc.. It received FDA 510(k) clearance on 2025-04-14 under 510(k) number K250802. The device is classified under product code MLR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the STERRAD® 100NX Sterilizer with ALLClear™ Technology (10104)?

STERRAD® 100NX Sterilizer with ALLClear™ Technology (10104) is a medical device that received FDA 510(k) clearance on 2025-04-14. The listed applicant is Advanced Sterilization Products, Inc.. The 510(k) number is K250802.

When did STERRAD® 100NX Sterilizer with ALLClear™ Technology (10104) receive FDA 510(k) clearance?

STERRAD® 100NX Sterilizer with ALLClear™ Technology (10104) received FDA 510(k) clearance on 2025-04-14, under 510(k) number K250802.

Who is the listed applicant for STERRAD® 100NX Sterilizer with ALLClear™ Technology (10104)?

The FDA 510(k) record lists Advanced Sterilization Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STERRAD® 100NX Sterilizer with ALLClear™ Technology (10104)?

The FDA product code for STERRAD® 100NX Sterilizer with ALLClear™ Technology (10104) is MLR.

列明Advanced Sterilization Products, 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。

K252843STERRAD 100NX 消毒系统，配备 ALLClear 技术（10104）K234084STERRAD® 化学指示剂（CI）条带（14100）；STERRAD® SEALSURE® 化学指示剂（CI）胶带（14202NL）；STERRAD VELOCITY® 生物指示剂（BI）（43210）（60个）；STERRAD VELOCITY® 生物指示剂（BI）（43210-30）（30个）；STERRAD VELOCITY® 阅读器（43220）；ULTRA GI® 过程挑战装置（PCD）（43400）（30个）K220404STERRAD NX 配备 ALLClear 技术 K212174STERRAD 100NX 消毒器，配备 ALLClear 技术

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。