Medical Device Manufacturer · US , Ann Arbor , MI

Cibernet Systems Corp. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2005

Recent clearances: MEDSTAR 220, MODEL 533-220

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Cibernet Systems Corp. Cardiovascular ✕

1 devices

1-1 of 1

Cleared Jul 19, 2005

MEDSTAR 220, MODEL 533-220

Cardiovascular · 95d