Q-Life Systems, 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) | K915231 | EPIDURAL INDICATION FOR VOLUMETRIC INFUSION PUMPS | FRN | 1992-01-22 | View |
| 510(k) | K896717 | PARTNER INFUSION SYSTEM: | FRN | 1990-08-02 | View |
No matching devices.
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