Brimms, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K842788 | DIFFERENTIAL DIAG. OCCLUSAL APPLIANCE | JXL | 1984-09-11 | View |
| 510(k) | K831344 | DIFFERENTIA/DIAGNOSTIC OCCLUSA/APPLIANC | 1983-07-18 | View |
No matching devices.
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