The following data is part of a premarket notification filed by Tecnomed, Inc. with the FDA for Hilo Trans-x Trauma Transport.
| Device ID | K792326 |
| 510k Number | K792326 |
| Device Name: | HILO TRANS-X TRAUMA TRANSPORT |
| Classification | Table, Radiographic, Tilting |
| Applicant | TECNOMED, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IXR |
| CFR Regulation Number | 892.1980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-11-19 |
| Decision Date | 1980-01-28 |