FDA 510(k), K212143, Neteera 130H/131H Vital Sign Monitoring Sensor

FDA 510(k), K212143, Neteera 130H/131H Vital Sign Monitoring Sensor

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510(K) Number: K212143
Device Name: Neteera 130H/131H Vital Sign Monitoring Sensor
Manufacturer: Neteera Technologies Ltd.
Device Classification Name: Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
Regulation Number: 870.2300
Classification Product Code: DRT
Date Received: 07/09/2021
Decision Date: 09/28/2022
Regulation Medical Specialty: Cardiovascular

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