Medical Device Manufacturer · US , Minneapolis, , MN

Cefar Medical AB - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002

Recent clearances: CEFAR REHAB 2 AND REHAB 2 PRO, CEFAR MEDICAL AB CEFAR PRIMO

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Cefar Medical AB Neurology ✕

1 devices

1-1 of 1

Cleared Jun 10, 2002

CEFAR MEDICAL AB CEFAR PRIMO

Neurology · 90d