Imediplus, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Cardiart Electronic Stethoscope Model DS101 Omni-Steth Electronic Stethoscope Model Omni-Steth, Electronic Stethoscope DS3011A
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Imediplus, Inc. Cardiovascular ✕
3 devices