PMA supplement
P050014 S001: FUJI COMPUTED RADIOGRAPHY MAMMOGRAPHY SUITE
FDA PMA supplement · Real-Time Process · Fujifilm Medical System U.S.A., Inc.
Key facts
| Original PMA | P050014 |
|---|---|
| Supplement number | S001 |
| Supplement type | Real-Time Process |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | FUJI COMPUTED RADIOGRAPHY MAMMOGRAPHY SUITE |
| Generic name | Full field digital, system, x-ray, mammographic |
| Applicant | Fujifilm Medical System U.S.A., Inc. |
| Product code | MUE |
| Received date | Oct 28, 2008 |
| Decision date | Jan 9, 2009 |
At a glance
- No Expedited review granted
- No Approval order on file
- No Summary of safety and effectiveness on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA supplements
A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: