Lorad Medical Systems, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K921962 | LORAD DIGITAL SPOT MAMMOGRAPHY | November 23, 1992 |
| K922619 | DIGITIZER, MODEL # 3-000A-1518 | July 1, 1992 |
| K913732 | MAMMOGRAPHIC X-RAY SYSTEM | February 3, 1992 |
| K913478 | RADIOGRAPHIC FILM MARKING SYSTEM | October 15, 1991 |
| K894935 | S-70 PORTABLE DENTAL X-RAY SYSTEM | April 25, 1990 |
| K894643 | RT-125 ROUGH TERRAIN MOBILE X-RAY UNIT | December 14, 1989 |
| K882875 | STEREOTACTIC BREAST LESION LOCALIZATION ACCESSORY | November 7, 1988 |
| K842102 | LORAD | July 17, 1984 |