Merck Millipore Ltd.

FDA Regulatory Profile

Summary

Total Recalls
1
510(k) Clearances
2
Inspections
1
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-0489-2019Class IIMinicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 May 14, 2018

Recent 510(k) Clearances

K-NumberDeviceDate
K143583Cathivex ¿GV filter unitsAugust 11, 2015
K133004VENTED MILLEX -GV, CATHIVEX -GVMarch 27, 2014