FDA 510(k) Applications Submitted by LINDSEY RONNENBERG
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K102758 | 09/23/2010 | TRULIGHT 5520 AND TRULIGHT 5320 | TRUMPF KREUZER MEDIZIN SYSTEME GMBH + CO.KG |
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