Electro-Diagnostic Imaging, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K003442 | MODIFICATION TO EDI VERIS SYSTEM | HLX | 2001-05-04 | View |
| 510(k) | K983983 | EDI VERIS SYSTEM | HLX | 1999-02-03 | View |
No matching devices.
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