FDA 510(k) Applications Submitted by HANJIN DIGI-X CO., LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K092772 | 09/09/2009 | PORTABLE X-RAY SYSTEM, MODEL HAND-RAY | HANJIN DIGI-X CO., LTD. |
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