Avery Dennison Corporation
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest Approval2017-03-29
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K163529 | ReliaTect Post-Op Dressing with CHG (8cm x 15cm), ReliaTect Post-Op Dressing with CHG (10cm x 25cm) | FRO | 2017-03-29 | View |
No matching devices.