Viasys Neuro Care is one of 24282 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Viasys Neuro Care - FDA 510(k) Cleared Devices
Recent clearances: NICOLETONE SYSTEM V32 AMPLIFIER, PIONEER TC8080, COMPANION III
2
Total
2
Cleared
0
Denied
Viasys Neuro Care has 2 FDA 510(k) cleared medical devices. Based in Stoughton, US.
Historical record: 2 cleared submissions from 2006 to 2006. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Viasys Neuro Care Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Viasys Neuro Care
2 devices