Jamieson Film Co.
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K970738 | KODAK DIGITAL SCIENCE CARDIAC DIGITAL ACQUISITION UNIT | IZI | 1997-05-07 | View |
| 510(k) | K971128 | CAP-35B III/CINE 275 | IXR | 1997-04-28 | View |
| 510(k) | K963334 | JAMIESON MODEL 2100 CINE FILM PROCESSOR AND KODAK CINEFLURE PROCESSOR MODEL 2100 | IXX | 1996-09-11 | View |
| 510(k) | K960043 | KODAK CARDIOLOGY DIGITAL ARCHIVE & REVIEW SYSTEM | LLZ | 1996-03-27 | View |
| 510(k) | K953563 | VANGUARD XR-350 CINEANGIOGRAM PROJECTOR | IZI | 1995-10-05 | View |
| 510(k) | K913241 | JAMIESON JT-CRP CINE FILM PROCESSOR | IXX | 1991-09-24 | View |
No matching devices.
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