Medical Device Manufacturer · US , Milford , MA

Micromass, Inc.

1 submissions · 1 cleared · Since 2001
1
Total
1
Cleared
0
Denied

Micromass, Inc. — FDA 510(k) Submissions

Micromass, Inc. has submitted 1 FDA 510(k) premarket notifications since 2001, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Ninhydrin And L-leucyl-l-alanine (fluorimetric), Phenylalanine . Use the specialty filter in the sidebar to narrow results.

1 devices
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