Medical Device Manufacturer · FI , 20101 Turku

Orion Corp. - FDA 510(k) Cleared Devices

21 submissions · 20 cleared · Since 1985

Recent clearances: RUBALEX, MODIFICATION, RESUBMITTED MODIFIED RUBALEX, RESUBMITTED SCANORA

View 21 510(k) Devices ↓

21

Total

20

Cleared

0

Denied

FDA 510(k) Regulatory Record - Orion Corp. Radiology ✕

4 devices

1-4 of 4

Cleared Mar 16, 1989

RESUBMITTED SCANORA

Radiology · 129d

Cleared Jun 10, 1988

Radiology · 60d

Cleared Jun 10, 1988

MAMEX DC MAG MG12

Radiology · 60d

Cleared Nov 23, 1987

MAMEX DC S SL10/MG14

Radiology · 49d