Automatic Film Processorio M. R80

No FDA recalls on record, checked 10 Oct 2026.

510(k) Number

K781068 ↗

FDA Product Code

IWX

Device Class

Class I

Regulation

21 CFR Part 892.6500

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

• Allmec 90/15

  Class II

  FDA 510(k) K811196 Active Cleared 9 Jun 1981

• Ralco Collimators, Manual, Radiographic

  Not classified

  FDA 510(k) K827125 Active Cleared 4 Mar 1982

• Ralco Collimators, Manual Radiographic

  Class II

  FDA 510(k) K820305 Active Cleared 4 Mar 1982

• Plurimat;radiographic Tube Mount

  Class I

  FDA 510(k) K781065 Active Cleared 17 Jul 1978

• Argostat

  Class I

  FDA 510(k) K811195 Active Cleared 9 Jun 1981

• Ralco Collimator, Automatic Radiographic

  Class II

  FDA 510(k) K820306 Active Cleared 5 Mar 1982

See all devices from Tecnomed, Inc. →