Lorad, A Hologic Co.
Lorad, A Hologic Co. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 11, 2013.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K122836 | AFFIRM BREAST BIOPSY GUIDANCE SYSTEM | January 11, 2013 |
| K071542 | DIGITAL STEREOLOC II | July 5, 2007 |
| K030666 | MULTICARE PLATINUM SYSTEM AND ACCESSORIES | March 25, 2003 |
| K013290 | MODIFIED 650 MAMMOGRAPHY SYSTEM | October 24, 2001 |
| K011987 | MODIFIED M-IV MAMMOGRAPHY SYSTEM | July 11, 2001 |