The following data is part of a premarket notification filed by Shimadzu Medical Systems with the FDA for Mu125m Mobile X-ray System.
| Device ID | K920393 |
| 510k Number | K920393 |
| Device Name: | MU125M MOBILE X-RAY SYSTEM |
| Classification | System, X-ray, Photofluorographic |
| Applicant | SHIMADZU MEDICAL SYSTEMS 101 WEST WALNUT ST. Gardenia, CA 90248 |
| Contact | De Mint |
| Correspondent | De Mint SHIMADZU MEDICAL SYSTEMS 101 WEST WALNUT ST. Gardenia, CA 90248 |
| Product Code | IZG |
| CFR Regulation Number | 892.1730 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-01-30 |
| Decision Date | 1992-04-06 |