Arco Medical Products Co. - FDA 510(k) Cleared Devices
Recent clearances: MODEL 3003 UNIPOLAR DEMAND CARDIAC GEN., EXTERNAL SILASTIC BOOT FOR CARDIAC PULSE, PROGRAMMABLE BIPOLAR CARDIAC GENERATOR
21
Total
20
Cleared
0
Denied
FDA 510(k) Regulatory Record - Arco Medical Products Co. General Hospital ✕
1 devices