The following data is part of a premarket notification filed by Eastman Kodak Company with the FDA for Kodak Ektachem Dt Slides (fe).
| Device ID | K934358 |
| 510k Number | K934358 |
| Device Name: | KODAK EKTACHEM DT SLIDES (FE) |
| Classification | Resin, Ion-exchange, Ascorbic Acid, Colorimetry, Iron Binding Capacity |
| Applicant | EASTMAN KODAK COMPANY 100 INDIGO CREEK DR. Rochester, NY 14652 -0882 |
| Contact | Yvonne E Middlefell |
| Correspondent | Yvonne E Middlefell EASTMAN KODAK COMPANY 100 INDIGO CREEK DR. Rochester, NY 14652 -0882 |
| Product Code | JQE |
| CFR Regulation Number | 862.1415 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-09-08 |
| Decision Date | 1994-03-21 |