Bioject, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K090003ZETAJETApril 2, 2009
K050734COOL.CLICKJune 3, 2005
K010623RECONSTITUTION KIT & VIAL CONNECTORApril 5, 2001
K003908SEROJETMarch 8, 2001
K994384CLICKERJune 22, 2000
K960373BIOJECTOR 2000 MODEL 1B02000March 5, 1997
K963012BIOJECT NEEDLE-FREE VIAL ADAPTER (13MM)October 15, 1996
K920631BIOJECT JET INJECTION SYSTEMJune 28, 1994
K861687BIOJECTOR SYRINGE SYSTEMApril 23, 1987