Medical Device Manufacturer · SE , Sweden

Aragona AB Co. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1987

Total

Cleared

Denied

Aragona AB Co. has 1 FDA 510(k) cleared medical devices. Based in Sweden, SE.

Historical record: 1 cleared submissions from 1987 to 1987. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Aragona AB Co. Filter by specialty or product code using the sidebar.

Aragona AB Co. is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Aragona AB Co.

1 devices

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