FR6000 FLOWMETER
Jan 1989
48d
Key Instruments
1
Total
1
Cleared
0
Denied
Key Instruments — FDA 510(k) Submissions
Key Instruments has submitted 1 FDA 510(k) premarket notifications since 1989, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Flowmeter, Tube, Thorpe, Back-pressure Compensated . Use the specialty filter in the sidebar to narrow results.
1 devices