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Axon Instruments, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K990683AXON MP-1 MICROPOSITIONERNovember 3, 1999
K970943GUIDELINE SYSTEMAugust 18, 1997
K971318MM-1 MOVEMENT MONITORJuly 28, 1997