The following data is part of a premarket notification filed by Mrx Corp. with the FDA for Mrx-750.
| Device ID | K933162 |
| 510k Number | K933162 |
| Device Name: | MRX-750 |
| Classification | Assembly, Tube Housing, X-ray, Diagnostic |
| Applicant | MRX CORP. 320 WESTWAY PL., SUITE 520 Arlington, TX 76018 |
| Contact | Don Darrow |
| Correspondent | Don Darrow MRX CORP. 320 WESTWAY PL., SUITE 520 Arlington, TX 76018 |
| Product Code | ITY |
| CFR Regulation Number | 892.1760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-06-29 |
| Decision Date | 1993-10-07 |