FDA 510(k) Applications Submitted by SCANDIMED. A.S.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K031238 | 04/18/2003 | VARICES NEEDLE | SCANDIMED. A.S. |
| K031236 | 04/18/2003 | AUTO-BAND LIGATOR | SCANDIMED. A.S. |
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