Reproductive Research Technologies, LP is one of 5195 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
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.
Reproductive Research Technologies, LP — FDA 510(k) Products and Clearance History
2 devices
Cleared
Jun 28, 2013
SURECALL LABOR MONITOR
Obstetrics & Gynecology
177d
Cleared
Jan 25, 2011
SURECALL EMG LABOR MONITOR
Obstetrics & Gynecology
734d