Medical Device Manufacturer · US , Miami , FL

Monica Veytia - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2008

Recent clearances: KANTERON DICOM STATION (KDS), MODEL 3.0

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Monica Veytia Radiology ✕

1 devices

1-1 of 1

Cleared Mar 19, 2008

KANTERON DICOM STATION (KDS), MODEL 3.0

Radiology · 127d