The following data is part of a premarket notification filed by Ohio Nuclear, Inc. with the FDA for Rad. Therapy Planning Sup. Sys..
| Device ID | K772305 |
| 510k Number | K772305 |
| Device Name: | RAD. THERAPY PLANNING SUP. SYS. |
| Classification | System, X-ray, Tomography, Computed |
| Applicant | OHIO NUCLEAR, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JAK |
| CFR Regulation Number | 892.1750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-12-14 |
| Decision Date | 1978-01-09 |