Medical Device Manufacturer · SE , 191 47 Sollentuna

Arlanda Medicinska Instrument Co. AB - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1997

Recent clearances: INTRACAVITY NEEDLE GUIDE KIT

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Arlanda Medicinska Instrument Co. AB Radiology ✕

1 devices

1-1 of 1

Cleared Jul 30, 1997

INTRACAVITY NEEDLE GUIDE KIT

Radiology · 595d