Cape Tech Medical Products
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) | K926038 | FLEX-TECH BALLOON DILATOR | KNQ | 1993-10-25 | View |
| 510(k) | K926039 | GUIDE-TECH ENCAPSULATED GUIDEWIRE | KNY | 1993-08-05 | View |
| 510(k) | K926040 | HELI-TECH RETRIEVAL BASKET | LQR | 1992-12-23 | View |
No matching devices.
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