Deltex Medical

FDA Regulatory Profile

Deltex Medical appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 8, 2006.

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