Rose K International , Ltd. is one of 14 FDA 510(k) medical device manufacturers from New Zealand in the dataset, ranked by real submission volume.
Rose K International , Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Rose K International , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Hamilton, NZ.
Historical record: 2 cleared submissions from 1995 to 2002. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Rose K International , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rose K International , Ltd.
2 devices