Medical Device Manufacturer · US , Danbury , CT

Lorad, A Hologic Co. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2001
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Lorad, A Hologic Co. Radiology ✕
5 devices
1-5 of 5
Cleared Jan 11, 2013
AFFIRM BREAST BIOPSY GUIDANCE SYSTEM
K122836 · IZH
Radiology · 116d
Cleared Jul 05, 2007
DIGITAL STEREOLOC II
K071542 · IZH
Radiology · 30d
Cleared Mar 25, 2003
MULTICARE PLATINUM SYSTEM AND ACCESSORIES
K030666 · IZH
Radiology · 22d
Cleared Oct 24, 2001
MODIFIED 650 MAMMOGRAPHY SYSTEM
K013290 · IZH
Radiology · 22d
Cleared Jul 11, 2001
MODIFIED M-IV MAMMOGRAPHY SYSTEM
K011987 · IZH
Radiology · 15d
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