FDA 510(k)

ivWatch Model 400，设备附件：扩展模块，SmartTouch传感器，患者电缆

K号: K192385 · 2020-07-02

决定日期2020-07-02

产品代码PMS

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

ivWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor, Patient Cable is the device name listed in this FDA 510(k) record. The listed applicant is Ivwatch, LLC. It received FDA 510(k) clearance on 2020-07-02 under 510(k) number K192385. The device is classified under product code PMS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ivWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor, Patient Cable?

ivWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor, Patient Cable is a medical device that received FDA 510(k) clearance on 2020-07-02. The listed applicant is Ivwatch, LLC. The 510(k) number is K192385.

When did ivWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor, Patient Cable receive FDA 510(k) clearance?

ivWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor, Patient Cable received FDA 510(k) clearance on 2020-07-02, under 510(k) number K192385.

Who is the listed applicant for ivWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor, Patient Cable?

The FDA 510(k) record lists Ivwatch, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ivWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor, Patient Cable?

The FDA product code for ivWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor, Patient Cable is PMS.

列明Ivwatch, LLC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。

K233881ivWatch® 型号 400 K222212ivWatch型号400 K162478ivWatch K153605ivWatch型号400

官方来源

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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。