Akron Catheter, Inc.
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) | K864736 | AKRO-SIL PLUS | KOD | 1986-12-24 | View |
| 510(k) | K823428 | KELLY INFLATABLE T DRAIN | FGE | 1983-01-18 | View |
| 510(k) | K760440 | CATHETER, NATURAL LATEX URETHRAL | KOD | 1976-10-20 | View |
No matching devices.
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