Invoclar North America, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K932774 | DW232 #31 | EJT | 1993-10-20 | View |
| 510(k) | K920560 | DW236-34 ALLOY FOR PORCELAIN FUSED TO METAL | EJS | 1992-03-02 | View |
No matching devices.
Advertisement