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Lorad, A Hologic Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K122836AFFIRM BREAST BIOPSY GUIDANCE SYSTEMJanuary 11, 2013
K071542DIGITAL STEREOLOC IIJuly 5, 2007
K030666MULTICARE PLATINUM SYSTEM AND ACCESSORIESMarch 25, 2003
K013290MODIFIED 650 MAMMOGRAPHY SYSTEMOctober 24, 2001
K011987MODIFIED M-IV MAMMOGRAPHY SYSTEMJuly 11, 2001