Jetprep, Ltd. is one of 15062 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Jetprep, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: JETPREP FLUSHING DEVICE OL-103037, JETPREP FLUSHING DEVICE OL-133037, JETPREP FLUSHING DEVICE OL-168037, JETPREP FLUSHIN, JETPREP FLUSHING DEVICE OL-103037 / OL-133037 / OL-168037 / PE-105038 / PE-150038 / PE-170038 / FU-169038
2
Total
2
Cleared
0
Denied
Jetprep, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 2 cleared submissions from 2012 to 2012. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Jetprep, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Jetprep, Ltd.
2 devices