Reproductive Research Technologies, LP is one of 24371 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Reproductive Research Technologies, LP - FDA 510(k) Cleared Devices
Recent clearances: SURECALL LABOR MONITOR, SURECALL EMG LABOR MONITOR
2
Total
2
Cleared
0
Denied
Reproductive Research Technologies, LP has 2 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 2 cleared submissions from 2011 to 2013. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Reproductive Research Technologies, LP Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Reproductive Research Technologies, LP
2 devices