FDA 510(k) Applications Submitted by INMED LTDA.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K030081 | 01/09/2003 | CSF400 AND CSF600 | INMED LTDA. |
| K030887 | 03/21/2003 | LEKTROGEL, MODEL LK3001 | INMED LTDA. |
| K030889 | 03/21/2003 | ULTRAEKOGEL MODELS EK 2000 & EK 2001 | INMED LTDA. |
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