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Ivwatch, LLC

6 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
ivWatch® Model 400 (K233881)Ivwatch, LLC2024-03-15
ivWatch Model 400 (K222212)Ivwatch, LLC2022-08-24
ivWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor, Patient Cable (K192385)Ivwatch, LLC2020-07-02
ivWatch (K162478)Ivwatch, LLC2016-12-22
ivWatch Model 400 (K153605)Ivwatch, LLC2016-02-11
ivWatch Model 400 (K142374)Ivwatch, LLC2015-02-13

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