Key Instruments is one of 20072 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Key Instruments - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Key Instruments has 1 FDA 510(k) cleared medical devices. Based in Trevose, US.
Historical record: 1 cleared submissions from 1989 to 1989. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Key Instruments Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Key Instruments
1 devices