Medical Device Manufacturer · CA , Toronto

Luminex Corp.

3 submissions · 3 cleared · Since 2008
3
Total
3
Cleared
0
Denied

Luminex Corp. — FDA 510(k) Submissions

Luminex Corp. has submitted 3 FDA 510(k) premarket notifications since 2008, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Instrumentation For Clinical Multiplex Test Systems . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
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All3 Chemistry 1 Immunology 1 Pathology 1