Minnesota Valley Engineering, Inc.
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) | K882328 | HI FLOW 50 | BYJ | 1988-06-28 | View |
| 510(k) | K875352 | HI FLOW PORTABLE LIQUID OXYGEN UNIT | BYJ | 1988-02-29 | View |
| 510(k) | K880101 | LIBERATOR 53/STROLLER 50 | BYJ | 1988-02-29 | View |
| 510(k) | K872449 | NOMAD (BASE UNIT/PORTABLE UNIT) | BYJ | 1987-07-21 | View |
No matching devices.
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