FDA 510(k) Applications Submitted by KIRCHNER & WILHELM GMBH + CO.KG
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K070270 | 01/29/2007 | PICCOLIGHT E50,PICCOLIGHT E56,EUROLIGHT E10, EUROLIGHT E30, AND EUROLIGHT E36 | KIRCHNER & WILHELM GMBH + CO.KG |
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