FDA 510(k) Applications Submitted by AGFA CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K052251 | 08/18/2005 | DRYSTAR MODEL 5500 | AGFA CORPORATION |
| K053634 | 12/29/2005 | COMPUTED RADIOGRAPHY SYSTEM WITH NX 1.0 WORKSTATION | AGFA CORPORATION |
| K062742 | 09/14/2006 | CR 85-X | AGFA CORPORATION |
| K062223 | 08/02/2006 | AGFA MODEL CR30-X | AGFA CORPORATION |
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