Tempus LS - Manual
Jul 2020
115d
Remote Diagnostic Technologies, Ltd. A Philips Company
1
Total
1
Cleared
0
Denied
Remote Diagnostic Technologies, Ltd. A Philips Company — FDA 510(k) Submissions
Remote Diagnostic Technologies, Ltd. A Philips Company has submitted 1 FDA 510(k) premarket notifications since 2020, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Dc-defibrillator, Low-energy, (including Paddles) . Use the specialty filter in the sidebar to narrow results.
1 devices