Smec, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K840367 | PRESSURE TRIGGER MOD OF SMEC INTRA-AORT | DSP | 1985-12-11 | View |
| 510(k) | K840037 | MODIFIED SMEC PERCUTANEOUS INTRA-AORTIC | DSP | 1985-02-01 | View |
| 510(k) | K832753 | PERCUTANEOUS BALLOON | DSP | 1984-10-13 | View |
| 510(k) | K823739 | INTRA-AORTIC BALLOON SYSTEM | DSP | 1983-02-18 | View |
| 510(k) | K823177 | SMEC BALLOON SYSTEM | DSP | 1982-12-15 | View |
| 510(k) | K813355 | MODIFICATION OF THE PERCUTAN-BALLOON | DSP | 1982-07-02 | View |
| 510(k) | K790755 | SMEC BALLOON CANNULA | DSP | 1980-05-14 | View |
No matching devices.
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