Medical Device Manufacturer · NZ , Hamilton

Rose K International , Ltd. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1995

Recent clearances: ROSE K POST GRAFT LENS, ROSE K LENS

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Rose K International , Ltd. Ophthalmic ✕

2 devices

1-2 of 2

Cleared May 30, 2002

ROSE K POST GRAFT LENS

Ophthalmic · 206d

Cleared Feb 07, 1995

Ophthalmic · 63d