ActiSpec Activity Monitor
Aug 2015
258d
Sleep Modus, Inc.
1
Total
1
Cleared
0
Denied
Sleep Modus, Inc. — FDA 510(k) Submissions
Sleep Modus, Inc. has submitted 1 FDA 510(k) premarket notifications since 2015, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Exerciser, Measuring . Use the specialty filter in the sidebar to narrow results.
1 devices