Rose K International , Ltd.

Rose K International , Ltd. holds 2 FDA 510(k) medical device clearances, first cleared 1995, most recent 2002.

Top product codes for Rose K International , Ltd.

HQD — Ophthalmic2 devices

Recent clearances by Rose K International , Ltd.

K013646 — ROSE K POST GRAFT LENSCode HQD·2002-05-30
K945955 — ROSE K LENSCode HQD·1995-02-07

Data sourced from openFDA. This site is unofficial and independent of the FDA.