Obmedical Company is one of 14060 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Obmedical Company - FDA 510(k) Cleared Devices
Recent clearances: LaborView™ LV1000 Wireless Electrode System, LaborView LV1000
2
Total
2
Cleared
0
Denied
Obmedical Company has 2 FDA 510(k) cleared medical devices. Based in Newberry, US.
Historical record: 2 cleared submissions from 2015 to 2020. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Obmedical Company Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Promedic, Inc. as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Obmedical Company
2 devices