Sensacare , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: SENSACARE MODEL SAA-102 ARM TYPE DIGITAL BLOOD PRESSURE MONITOR, SENSACARE SAW-102 WRIST DIGITAL BLOOD PRESSURE MONITOR
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Sensacare , Ltd. Cardiovascular ✕
2 devices