Bioject Medical Technologies, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K121270BIOJECT NEEDLE-FREE INJECTION MANAGEMENT SYSTEMJuly 19, 2012
K043304Q-CAP NEEDLE-FREE RECONSTITUTION 13MM VIAL ADAPTER, MODEL 6100-01January 14, 2005
K041564Q-CAP NEEDLE-FREE RECONSTITUTION 13MM VIAL ADAPTER, MODEL 6100-01July 16, 2004