iotaSOFT® 插入系统
K号: K252339 · 2026-01-09
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决定日期2026-01-09
产品代码QQH
咨询委员会医疗设备监管文本描述翻译如下：
关于[公司/产品名称]的监管信息：
- 美国食品药品监督管理局（FDA）批准号：[510(k)编号]
- 预市场批准（PMA）申请号：[PMA编号]
- 临床试验注册号（NCT）：[NCT编号]
- 医学文献标识符（PMID）：[PMID编号]
- 产品标识符：[标识符]
- 相关政策：医疗监管政策v1
- 更多信息请访问：[URL]
请注意，以上翻译保留了公司/产品名称、FDA、510(k)、PMA、NCT、PMID、标识符和URL。
决定实质等同
器械摘要
iotaSOFT® Insertion System is the device name listed in this FDA 510(k) record. The listed applicant is Iotamotion, Inc.. It received FDA 510(k) clearance on 2026-01-09 under 510(k) number K252339. The device is classified under product code QQH. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the iotaSOFT® Insertion System?
iotaSOFT® Insertion System is a medical device that received FDA 510(k) clearance on 2026-01-09. The listed applicant is Iotamotion, Inc.. The 510(k) number is K252339.
When did iotaSOFT® Insertion System receive FDA 510(k) clearance?
iotaSOFT® Insertion System received FDA 510(k) clearance on 2026-01-09, under 510(k) number K252339.
Who is the listed applicant for iotaSOFT® Insertion System?
The FDA 510(k) record lists Iotamotion, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for iotaSOFT® Insertion System?
The FDA product code for iotaSOFT® Insertion System is QQH.
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。
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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