Medical Device Manufacturer · CZ , Prague

Hightech Development

1 submissions · 1 cleared · Since 2018
1
Total
1
Cleared
0
Denied

Hightech Development — FDA 510(k) Submissions

Hightech Development has submitted 1 FDA 510(k) premarket notifications since 2018, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Device, Iontophoresis, Other Uses . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
Filters
All1 Physical Medicine 1