FDA 510(k) Applications Submitted by GEORGE LEON
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K963334 | 08/26/1996 | JAMIESON MODEL 2100 CINE FILM PROCESSOR AND KODAK CINEFLURE PROCESSOR MODEL 2100 | JAMIESON FILM CO. |
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