Home / Companies / Millipore Corporation

Millipore Corporation

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K093815LIGHT DIAGNOSTICS HUMAN METAPNEUMOVIRUS DFA KIT, MODEL CATALOG NUMBER 3124March 12, 2010
K081527LIGHT DIAGNOSTICS HSV 1/2 TYPING DFA KITApril 1, 2009