Critikon Company, LLC - FDA 510(k) Cleared Devices
Recent clearances: DINAMAP PRO 1000 MONITOR, MODEL 1000, DINAMAP ADVANCED NIBP MODULE, DINAMAP PRO SERIES MONITOR, MODELS 100, 200, 300, 400
51
Total
51
Cleared
0
Denied
FDA 510(k) Regulatory Record - Critikon Company, LLC Gastroenterology & Urology ✕
1 devices