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-NumberDeviceDate
K921962LORAD DIGITAL SPOT MAMMOGRAPHYNovember 23, 1992
K922619DIGITIZER, MODEL # 3-000A-1518July 1, 1992
K913732MAMMOGRAPHIC X-RAY SYSTEMFebruary 3, 1992
K913478RADIOGRAPHIC FILM MARKING SYSTEMOctober 15, 1991
K894935S-70 PORTABLE DENTAL X-RAY SYSTEMApril 25, 1990
K894643RT-125 ROUGH TERRAIN MOBILE X-RAY UNITDecember 14, 1989
K882875STEREOTACTIC BREAST LESION LOCALIZATION ACCESSORYNovember 7, 1988
K842102LORADJuly 17, 1984