Nihon Kohden America, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NIHON KOHDEN EEG-1200A WITH JE-120A MULTI CHANNEL ELECTRODE JUNCTION BOX, NIHON KOHDEN QP-160 AK TREND PROGRAM WITH THE ADDITION OF DSA ASYMMETRY TREND AND FFT P, NIHON KOHDEN QP-160AK EEG TREND PROGRAM
166
Total
163
Cleared
0
Denied
FDA 510(k) Regulatory Record - Nihon Kohden America, Inc. Gastroenterology & Urology ✕
1 devices