Pro Design Intl. AS is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pro Design Intl. AS - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Pro Design Intl. AS has 2 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 2 cleared submissions from 1984 to 1984. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Pro Design Intl. AS Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pro Design Intl. AS
2 devices