Medical Device Manufacturer · US , New York , NY

Kardiosis Ltd. Co. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1992

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Kardiosis Ltd. Co. Cardiovascular ✕

1 devices

1-1 of 1

Cleared Mar 30, 1992

ARS-EKG 12K INTERPRETIVE ELECTROCARDIOGRAPHY SYST

Cardiovascular · 193d