Millipore Corporation is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Millipore Corporation - FDA 510(k) Cleared Devices
Recent clearances: LIGHT DIAGNOSTICS HUMAN METAPNEUMOVIRUS DFA KIT, MODEL CATALOG NUMBER 3124, LIGHT DIAGNOSTICS HSV 1/2 TYPING DFA KIT
2
Total
2
Cleared
0
Denied
Millipore Corporation has 2 FDA 510(k) cleared medical devices. Based in Temecula, US.
Historical record: 2 cleared submissions from 2009 to 2010. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Millipore Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Millipore Corporation
2 devices