Jamieson Model 2100 Cine Film Processor and Kodak Cineflure Processor Model 2100

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K963334 ↗

FDA Product Code

IXX

Device Class

Class II

Regulation

21 CFR Part 892.1900

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

• Jamieson Jt-Crp Cine Film Processor

  Class II

  FDA 510(k) K913241 Active Cleared 24 Sep 1991

• Kodak Digital Science Cardiac Digital Acquisition Unit

  Class II

  FDA 510(k) K970738 Active Cleared 7 May 1997

• Vanguard Xr-350 Cineangiogram Projector

  Class II

  FDA 510(k) K953563 Active Cleared 5 Oct 1995

• Cap-35B III/Cine 275

  Class II

  FDA 510(k) K971128 Active Cleared 28 Apr 1997

• Kodak Cardiology Digital Archive & Review System

  Class II

  FDA 510(k) K960043 Active Cleared 27 Mar 1996