Medical Device Manufacturer · US , Norton , OH

Wallac, Inc.

2 submissions · 1 cleared · Since 1999
2
Total
1
Cleared
1
Denied

Wallac, Inc. — FDA 510(k) Submissions

Wallac, Inc. has submitted 2 FDA 510(k) premarket notifications since 1999, of which 1 received clearance as substantially equivalent to a predicate device.

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

2 devices
1–2 of 2
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