Eschmann Bros. & Walsh , Ltd.
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) | K864637 | MODIFIED ESCHMANN DILATATION CATHETER | 1987-01-06 | View | |
| 510(k) | K852935 | ESCHMANN ELECTROSURGICAL UNIT, MODEL TD411 | GEI | 1985-10-10 | View |
| 510(k) | K781863 | DEVICE, FEMALE INCONTINENCE | HHW | 1978-11-06 | View |
No matching devices.
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