RGS; RGS Mini
Jun 2023
268d
Genesis Air, Inc.
1
Total
1
Cleared
0
Denied
Genesis Air, Inc. — FDA 510(k) Submissions
Genesis Air, Inc. has submitted 1 FDA 510(k) premarket notifications since 2023, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Purifier, Air, Ultraviolet, Medical . Use the specialty filter in the sidebar to narrow results.
1 devices