FDA 510(k) Applications Submitted by AVERY DENNISON CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K163529 | 12/16/2016 | ReliaTect Post-Op Dressing with CHG (8cm x 15cm), ReliaTect Post-Op Dressing with CHG (10cm x 25cm) | AVERY DENNISON CORPORATION |
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