Fischer-Zoth Audiologic Systems, 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) | K013977 | ECHO-SCREEN T, TA, TD, TDA, TC | GWJ | 2002-06-14 | View |
| 510(k) | K982642 | ECHO-SCREEN | EWO | 1998-10-21 | View |
No matching devices.
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