Medical Device Manufacturer · US , Arvada , CO

Collimare, LLC

1 submissions · 1 cleared · Since 2007
1
Total
1
Cleared
0
Denied

Collimare, LLC — FDA 510(k) Submissions

Collimare, LLC has submitted 1 FDA 510(k) premarket notifications since 2007, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Collimator, Automatic, Radiographic . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
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All1 Radiology 1