Nihon Kohden is one of 18553 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nihon Kohden - FDA 510(k) Cleared Devices
Recent clearances: Nihon Kohden CSM 1901 Bedside Monitor, NETKONNECT REMOTE NETWORK EXTENSION
2
Total
2
Cleared
0
Denied
Nihon Kohden has 2 FDA 510(k) cleared medical devices. Based in Foothill Ranch, US.
Historical record: 2 cleared submissions from 2011 to 2015. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Nihon Kohden Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Certified Compliance Solutions, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Nihon Kohden
2 devices