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Med-Conduit, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
2
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K062901
HEMOCATH II
February 8, 2007
K053123
PD CATH
March 29, 2006
K043292
HEMOCATH
March 16, 2005