Specialized Health Products International, 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) | K073050 | SAFESTEP MAX POWER-INJECTABLE INFUSION SET | FPA | 2008-01-25 | View |
| 510(k) | K070449 | LUMILOC (TM) SAFETY INTRODUCER NEEDLE | KNT | 2007-06-14 | View |
No matching devices.
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