Medical Device Manufacturer · US , North Billerica , MA

Magellan Diagnostics

2 submissions · 2 cleared · Since 2013
2
Total
2
Cleared
0
Denied

Magellan Diagnostics — FDA 510(k) Submissions

Magellan Diagnostics has submitted 2 FDA 510(k) premarket notifications since 2013, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Lead, Atomic Absorption . Use the specialty filter in the sidebar to narrow results.

2 devices
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All2 Chemistry 1 Toxicology 1