FDA 510(k) Applications Submitted by MANFRED BARTSCH-TITTMANN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K131959 | 06/27/2013 | HEINE MINI 3000(R) OPHTHALMOSCOPE | HEINE OPTOTECHNIK GMBH & CO. KG. |
| K131961 | 06/27/2013 | HEINE BETA 200(R) OPHTHALMOSCOPE | HEINE OPTOTECHNIK GMBH & CO. KG. |
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