Bosworth Co.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K991687 | MODIFICATION TO LINER II: SOFT RELINE LIQUID | EBI | 1999-10-07 | View |
| 510(k) | K991902 | LC PIT & FISSURE SEALANT | EBC | 1999-07-26 | View |
| 510(k) | K953119 | BOSWORTH RESIN II | EBI | 1995-08-28 | View |
| 510(k) | K810094 | DENTURE RUBBER BASE MATERIAL | EBI | 1981-02-02 | View |
No matching devices.
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