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Brainbase Corporation

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K083372ARROWBONE-A, ARROWBONE-BDecember 8, 2009
K063236BETA-POWDERFebruary 16, 2007
K052254MYTIS ARROW XXXXJune 1, 2006