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Dana Laboratories

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K854391HEMODIALYSIS CONCENTRATEJanuary 8, 1986
K851431HEMODIALYSIS CONCENTRATE ADDITIVESJune 12, 1985