Jamieson Film Co.
Dallas, TX, US
Jamieson Film Co. appears in FDA device records in Dallas, TX. FDA records list 6 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 6
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 6 510(k) clearances for Jamieson Film Co. between 1991 and 1997. The busiest year on record is 1996, with 2. The most recent is 1997, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1991 | 1 |
| 1995 | 1 |
| 1996 | 2 |
| 1997 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K970738 | KODAK DIGITAL SCIENCE CARDIAC DIGITAL ACQUISITION UNIT | IZI | Substantially Equivalent | |
| K971128 | CAP-35B III/CINE 275 | IXR | Substantially Equivalent | |
| K963334 | JAMIESON MODEL 2100 CINE FILM PROCESSOR AND KODAK CINEFLURE PROCESSOR MODEL 2100 | IXX | Substantially Equivalent | |
| K960043 | KODAK CARDIOLOGY DIGITAL ARCHIVE & REVIEW SYSTEM | LLZ | Substantially Equivalent | |
| K953563 | VANGUARD XR-350 CINEANGIOGRAM PROJECTOR | IZI | Substantially Equivalent | |
| K913241 | JAMIESON JT-CRP CINE FILM PROCESSOR | IXX | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain