Medical Device Manufacturer · SE , Sweden

Synectics AB - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1984

Total

Cleared

Denied

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

Historical record: 1 cleared submissions from 1984 to 1984. Primary specialty: Gastroenterology & Urology.

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

Synectics AB 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 - Synectics AB

1 devices

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