Bioject Medical Technologies, Inc. is one of 21644 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bioject Medical Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BIOJECT NEEDLE-FREE INJECTION MANAGEMENT SYSTEM, Q-CAP NEEDLE-FREE RECONSTITUTION 13MM VIAL ADAPTER, MODEL 6100-01, Q-CAP NEEDLE-FREE RECONSTITUTION 13MM VIAL ADAPTER, MODEL 6100-01
3
Total
3
Cleared
0
Denied
Bioject Medical Technologies, Inc. has 3 FDA 510(k) cleared medical devices. Based in Bedminster, US.
Historical record: 3 cleared submissions from 2004 to 2012. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Bioject Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bioject Medical Technologies, Inc.
3 devices
Cleared
Jul 19, 2012
BIOJECT NEEDLE-FREE INJECTION MANAGEMENT SYSTEM
General Hospital
84d
Cleared
Jan 14, 2005
Q-CAP NEEDLE-FREE RECONSTITUTION 13MM VIAL ADAPTER, MODEL 6100-01
General Hospital
45d
Cleared
Jul 16, 2004
Q-CAP NEEDLE-FREE RECONSTITUTION 13MM VIAL ADAPTER, MODEL 6100-01
General Hospital
36d