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Dianon Systems, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K882105CODE #D2020-FINE NEEDLE ASPIRATION BIOPSY SYSTEMJuly 11, 1988
K872597FINE NEEDLE ASPIRATION BIOPSY SYSTEM-PROSTATEJuly 28, 1987