The following data is part of a premarket notification filed by Tecnomed, Inc. with the FDA for Plurix C; Radiographic Table.
| Device ID | K781066 |
| 510k Number | K781066 |
| Device Name: | PLURIX C; RADIOGRAPHIC TABLE |
| Classification | Table, Radiographic, Stationary Top |
| Applicant | TECNOMED, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IXQ |
| CFR Regulation Number | 892.1980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-06-26 |
| Decision Date | 1978-07-17 |