Medical Device Manufacturer · US , Temecula , CA

Millipore Corporation

2 submissions · 2 cleared · Since 2009
2
Total
2
Cleared
0
Denied

Millipore Corporation — FDA 510(k) Submissions

Millipore Corporation has submitted 2 FDA 510(k) premarket notifications since 2009, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Antisera, Fluorescent, Herpesvirus Hominis 1,2, Antisera, Fluorescent, Human Metapneumovirus . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Microbiology 2