FDA 510(k) Applications Submitted by BERCHTOLD GMBH & CO. KG
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K090378 | 02/17/2009 | CHROMOPHARE E 668 | BERCHTOLD GMBH & CO. KG |
| K120392 | 02/08/2012 | CHROMOPHARE F 628 AND F 528 | BERCHTOLD GMBH & CO. KG |
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