Fujifilm Medical Systems USA has received Food and Drug Administration 510(k) clearance to deploy its DryPix dry laser imagers for full-field digital mammography (FFDM) use.
The clearance covers the company’s DryPix 7000, DryPix 5000, and DryPix FM-DP L imagers, according to the Stamford, CT-based vendor.
By AuntMinnie.com staff writersJanuary 15, 2004
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