Medical Device Manufacturer · SE , Bromma

Icor AB - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1986

16

Total

16

Cleared

0

Denied

FDA 510(k) Regulatory Record - Icor AB Ophthalmic ✕

1 devices

1-1 of 1

Cleared Jun 23, 1992

BREATH-EASY, MODIFICATION

Ophthalmic · 272d