Pulse Scientific, 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) | K923768 | PULSE CRP TEST | DCK | 1992-12-01 | View |
| 510(k) | K923767 | PULSE IM RED CELL TEST | KTN | 1992-10-16 | View |
| 510(k) | K923771 | PULSE RF TEST | DHR | 1992-10-05 | View |
No matching devices.
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