The following data is part of a premarket notification filed by Rinn Corp. with the FDA for X-ray Co-ordinator.
| Device ID | K772313 |
| 510k Number | K772313 |
| Device Name: | X-RAY CO-ORDINATOR |
| Classification | Holder, Head, Radiographic |
| Applicant | RINN CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IWY |
| CFR Regulation Number | 892.1920 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-12-12 |
| Decision Date | 1978-01-30 |