Home / Companies / Dana Laboratories

Dana Laboratories

FDA Regulatory Profile

Dana Laboratories appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 8, 1986.

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

FDA data resources