The following data is part of a premarket notification filed by Atomic Products Corp. with the FDA for Radiographic Transport, Trauma Model 056-230, 235.
| Device ID | K904623 |
| 510k Number | K904623 |
| Device Name: | RADIOGRAPHIC TRANSPORT, TRAUMA MODEL 056-230, 235 |
| Classification | Table, Radiographic, Stationary Top |
| Applicant | ATOMIC PRODUCTS CORP. P.O. DRAWER R Shirley, NY 11967 |
| Product Code | IXQ |
| CFR Regulation Number | 892.1980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-10-11 |
| Decision Date | 1990-11-06 |