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Datrend Systems, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K062099
PHASE 3, MODEL DT-1
January 25, 2007
K980165
INFUTEST 2000 INFUSION DEVICE ANALYZER
April 20, 1998