Rapid Injection Systems Corp.
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) | K072479 | FLEXITE SUPREME, FLEXITE PLUS, FLEXITE M.P., NORTHERN AND FLEXITE PRO-GUARD | EBI | 2007-11-09 | View |
| 510(k) | K810869 | SILICONE ELASTOMER KIT | EBI | 1981-04-29 | View |
No matching devices.
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