FDA 510(k) Applications Submitted by THOMAS WEBER
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K121825 | 06/21/2012 | CS-MAG II | BIOMAGNETIK-PARK GMBH |
| K101892 | 07/07/2010 | HEINE GAMMA G7; HEINE GAMMA G5, HEINE GAMMA GP, HEINE GAMMA GST, HEINE GAMMA XXL LF MODEL M-000.09.23X, M-000.09.24X, M- | HEINE OPTOTECHNIK GMBH & CO. KG. |
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