FDA 510(k) Applications Submitted by FUJIFILM MEDICAL SYSTEMS, USA INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K110729 | 03/16/2011 | ASPIRE HD FULL-FIELD DIGITAL MAMMOGRAPHY SYSTEM | FUJIFILM MEDICAL SYSTEMS, USA INC. |
| K133972 | 12/26/2013 | ASPIRE CRISTALLE | FUJIFILM MEDICAL SYSTEMS, USA INC. |
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