Biodermis Corp.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K003948 | EPI-DERM SILICONE GEL SHEETING | MDA | 2001-01-29 | View |
| 510(k) | K992146 | SCARAID SILICONE GEL SHEETING | MDA | 1999-07-30 | View |
| 510(k) | K991604 | EPI-FOAM SILICONE SHEETING | MDA | 1999-06-09 | View |
| 510(k) | K964047 | CRYOSIL SILICONE GEL SHEETING | GEH | 1997-03-19 | View |
| 510(k) | K942156 | EPI-DERM SILICONE GEL SHEETING | MDA | 1994-06-13 | View |
No matching devices.
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