Medical Device Manufacturer · IL , Kfar Saba

Cardiosonix, Ltd. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2002

Recent clearances: QUANTIX OR VESSEL STABILIZER DEVICE, QUANTIX/OR DEVICE, QUANTIX/ND DEVICE

View 3 510(k) Devices ↓

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Cardiosonix, Ltd. Cardiovascular ✕

3 devices

1-3 of 3

Cleared Jun 07, 2004

QUANTIX OR VESSEL STABILIZER DEVICE

Cardiovascular · 32d

Cleared Aug 20, 2003

QUANTIX/OR DEVICE

Cardiovascular · 198d

Cleared Nov 13, 2002

QUANTIX/ND DEVICE

Cardiovascular · 29d