FDA 510(k) Applications Submitted by Orantech Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K182327 08/27/2018 Patient Cables and Leadwires , Disposable ECG Leadwires Orantech Inc.
K173194 10/02/2017 Temperature Probe Orantech Inc.
K181270 05/14/2018 Disposable SpO2 Sensors, Reusable SpO2 Sensors Orantech Inc.
K171828 06/20/2017 ETCO2 Sensor Orantech Inc.
K173197 10/02/2017 Reusable NIBP Cuff Orantech Inc.


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