FDA 510(k) Applications Submitted by LICHER MEDIZINTECHNOLOGIE GMBH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K062308 | 08/08/2006 | LMT-KATH-S; LMT-KATH-I | LICHER MEDIZINTECHNOLOGIE GMBH |
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