Bip USA, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K024089VACUFLASH BIOPSY SYSTEMMarch 11, 2003
K934371BIP MULTI MODIFICATIONApril 28, 1994
K934370BIP BIOPSY NEEDLE MODIFICATIONMarch 7, 1994
K935457LOCALIZATION WIRE OR MARKER - SURGICALFebruary 17, 1994
K925870SPACERMay 19, 1993
K925875HORIZONTAL NEEDLE GUIDE ATTACHMENTApril 6, 1993
K925874BREAST STABILIZERMarch 16, 1993