Persyst Development Corp.
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) | K132306 | PERSYST 12 EEG REVIEW AND ANALYSIS SOFTWARE | OMB | 2013-11-21 | View |
| 510(k) | K103103 | PRESSON ELECTRODE | GXZ | 2011-12-08 | View |
| 510(k) | K011397 | PERSYST REVEAL | OMB | 2001-08-03 | View |
| 510(k) | K974718 | PERSYST PRISM | GWS | 1998-03-09 | View |
No matching devices.
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