The following data is part of a premarket notification filed by Sybron Corp. with the FDA for Lf Motorized Radiographic Film Viewer.
| Device ID | K840607 |
| 510k Number | K840607 |
| Device Name: | LF MOTORIZED RADIOGRAPHIC FILM VIEWER |
| Classification | Illuminator, Radiographic-film |
| Applicant | SYBRON CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IXC |
| CFR Regulation Number | 892.1890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-02-13 |
| Decision Date | 1984-03-05 |