Monitored Therapeutics, Inc. is one of 14246 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Monitored Therapeutics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Dublin, US.
Historical record: 2 cleared submissions from 2017 to 2020. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Monitored Therapeutics, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by ProMedic, LLC and Monitored Therapeutics, Inc. C/O Promedic, LLC.
FDA 510(k) Regulatory Record - Monitored Therapeutics, Inc.
2 devices