Valley West, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K990447 | 1000 PRESSURE INFUSION SIGMACON 1000 | FRN | 1999-05-12 | View |
| 510(k) | K980089 | 3600 PRESURE INFUSOR, SIGMACON 3600, LAPRO FLOW 3000 | FRN | 1998-03-24 | View |
| 510(k) | K973814 | TRUMP-IT II AND MAGNUM 250 | GCJ | 1998-01-30 | View |
No matching devices.
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