# Jamieson Film Co.

- Location (FDA's records): Dallas, TX
- FDA decisions: 6 (1991–1997): 6 510(k) clearances
- Product codes: IZI (2), IXX (2), LLZ (1), IXR (1)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 4 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Arnold & Richter Cine Technik: 1 (https://510kreport.com/company/arnold-richter-cine-technik)
- Infimed, Inc.: 1 (https://510kreport.com/company/infimed)
- Heartware, Inc.: 1 (https://510kreport.com/company/heartware)

## Its most-cited devices
- K960043: Kodak Cardiology Digital Archive & Review System (1996), cited by 2
- K913241: Jamieson JT-CRP Cine Film Processor (1991), cited by 1
- K971128: Cap-35B Iii/Cine 275 (1997), cited by 1

## Recent decisions
- K970738: Kodak Digital Science Cardiac Digital Acquisition Unit (May 7, 1997)
- K971128: Cap-35B Iii/Cine 275 (Apr 28, 1997)
- K963334: Jamieson Model 2100 Cine Film Processor and Kodak Cineflure Processor Model 2100 (Sep 11, 1996)
- K960043: Kodak Cardiology Digital Archive & Review System (Mar 27, 1996)
- K953563: Vanguard XR-350 Cineangiogram Projector (Oct 5, 1995)
- K913241: Jamieson JT-CRP Cine Film Processor (Sep 24, 1991)

Source page: https://510kreport.com/company/jamieson-film