Glaxosmithkline Consumer Healthcare, L.P.
FDA 510(k) & PMA Approved Devices — 1 products
Advertisement
Total Devices1
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K041563 | OASIS DRY MOUTH RELIEF DISCS OR OASIS MOUTH MOISTURIZING DISCS | LFD | 2004-08-27 | View |
No matching devices.
Advertisement