Medical Device Manufacturer · US , Orlando , FL

Dial-A-Rad

1 submissions · 1 cleared · Since 1992
1
Total
1
Cleared
0
Denied

Dial-A-Rad — FDA 510(k) Submissions

Dial-A-Rad has submitted 1 FDA 510(k) premarket notifications since 1992, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Table, Radiographic, Stationary Top . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
Filters
All1 Radiology 1