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Deltex Medical

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K052989DP240 240 HOUR DOPPLER PROBEMarch 8, 2006
K031706CARDIOQ, MODEL 9051-7005August 6, 2003
K951369EDMNovember 7, 1995