Jostra Bentley is one of 22293 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Jostra Bentley - FDA 510(k) Cleared Devices
Recent clearances: HOLLOW FIBER MEMBRANE OYGENATOR QUADROX HMO 1010, JOSTRA HL-20 TWIN PUMP, JOSTRA HL-15 MODULAR HEART-LUNG MACHINE (HEREINAFTER CALLED THE HL-15 OR THE DEVICE
3
Total
3
Cleared
0
Denied
Jostra Bentley has 3 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 3 cleared submissions from 1995 to 1999. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Jostra Bentley Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Jostra Bentley
3 devices