The following data is part of a premarket notification filed by Lorad Corp. with the FDA for Lorad M-iv, Lorad M-ivi.
| Device ID | K945241 |
| 510k Number | K945241 |
| Device Name: | LORAD M-IV, LORAD M-IVI |
| Classification | System, X-ray, Mammographic |
| Applicant | LORAD CORP. 36 APPLE RIDGE RD. Danbury, CT 06810 |
| Contact | Marvin Rosenbaum |
| Correspondent | Marvin Rosenbaum LORAD CORP. 36 APPLE RIDGE RD. Danbury, CT 06810 |
| Product Code | IZH |
| CFR Regulation Number | 892.1710 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-10-27 |
| Decision Date | 1995-03-31 |