FDA 510(k) Applications Submitted by BEIERSDORF AG
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K022645 | 08/08/2002 | CURAD | BEIERSDORF AG |
| K032462 | 08/11/2003 | CURAD SILVER ACTIVE GEL BANDAGE | BEIERSDORF AG |
| K032463 | 08/11/2003 | CURAD SILVER BANDAGE | BEIERSDORF AG |
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