Coors Biomedical Co.
FDA 510(k) & PMA Approved Devices — 7 products
Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K863176 | ADDITIONAL CLINICAL USAGES FOR OSTEOGRAF/AR & AR+ | LYC | 1986-11-26 | View |
| 510(k) | K862324 | OSTEOGRAF/AR AND OSTEOGRAF/AR+ | LYC | 1986-08-15 | View |
| 510(k) | K862061 | OSTEOGRAF/AR+ PERMARIDGE HYDROXYLAPATITE, 18-40 | LYC | 1986-07-29 | View |
| 510(k) | K861084 | OSTEOGRAF/AR ALVEOLAR RID HYDROX, 18-40 MESH | LYC | 1986-04-30 | View |
| 510(k) | K861083 | OSTEOGRAF/AR+(PLUS) ALVEOLAR RID HYDROX 18-40 MESH | LYC | 1986-04-30 | View |
| 510(k) | K852742 | OSTEOGRAF AR ALVEOLAR RIDGE HYDROXYLAPATITE 18-40 | LYC | 1985-09-26 | View |
| 510(k) | K810822 | DENTAL PORCELAIN POWDER | EIH | 1981-04-21 | View |
No matching devices.