Medical Device Manufacturer · US , Chicago , IL

John O. Butler Co.

4 submissions · 3 cleared · Since 1995
4
Total
3
Cleared
0
Denied

John O. Butler Co. — FDA 510(k) Submissions

John O. Butler Co. has submitted 4 FDA 510(k) premarket notifications since 1995, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Toothbrush, Powered, Floss, Dental, Toothbrush, Manual . Use the specialty filter in the sidebar to narrow results.

4 devices
1–4 of 4
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All4 Dental 4