Kepler Medtec is one of 20310 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kepler Medtec - FDA 510(k) Cleared Devices
Recent clearances: KEPLER MEDTEC DISPOSABLE BIPOLAR CABLE, ECG SINGLE PATIENT USE LEAD WIRE SET, MODELS 2048801-5 TO 2048801-8
2
Total
2
Cleared
0
Denied
Kepler Medtec has 2 FDA 510(k) cleared medical devices. Based in Ashland, US.
Historical record: 2 cleared submissions from 2010 to 2011. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Kepler Medtec Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kepler Medtec
2 devices