FDA 510(k) Applications Submitted by MEDIEN INTERNATIONAL CO., LTD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K093816 | 12/11/2009 | DIGITAL RADIOGRAPHY SYSTEM, MODELS GALAXY 900 AND 1600 | MEDIEN INTERNATIONAL CO., LTD |
| K132921 | 09/17/2013 | GALAXY PLUS | MEDIEN INTERNATIONAL CO., LTD |
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