Stomavision (Stv)

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K951074 ↗

FDA Product Code

EIA

Device Class

Class I

Regulation

21 CFR Part 872.6640

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Stomavision (Stv)

  Class I

  FDA 510(k) K913464 Active Cleared 13 Nov 1991

• Atlantis

  Class II

  FDA 510(k) K953936 Active Cleared 28 Dec 1995

• Trophypan and Trophypan C

  Class II

  FDA 510(k) K033690 Active Cleared 20 Feb 2004

• Trophy Radiologie Rvg Portable Radiovisiography

  Class II

  FDA 510(k) K950532 Active Cleared 19 Apr 1995

• Trophy Radiologie Rvg Radiovisiography

  Class II

  FDA 510(k) K950533 Active Cleared 30 Jun 1995

• Modification to Digipan

  Class II

  FDA 510(k) K991912 Active Cleared 22 Jun 1999

See all devices from Trophy Radiologie →