CARDIOSPY ECG HOLTER SYSTEMS
Dec 2014
246d
Labtech Kft.
1
Total
1
Cleared
0
Denied
Labtech Kft. — FDA 510(k) Submissions
Labtech Kft. has submitted 1 FDA 510(k) premarket notifications since 2014, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Electrocardiograph, Ambulatory, With Analysis Algorithm . Use the specialty filter in the sidebar to narrow results.
1 devices