Medical Device Manufacturer · DK , Copenhagen

Multicept, Aps. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1985

Total

Cleared

Denied

Multicept, Aps. has 2 FDA 510(k) cleared medical devices. Based in Copenhagen, DK.

Historical record: 2 cleared submissions from 1985 to 1996. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Multicept, Aps. Filter by specialty or product code using the sidebar.

Multicept, Aps. is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Multicept, Aps.

2 devices

1-2 of 2