Kingston Technologies, Inc.
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K935232 | HYDROTORQUE GUIDE WIRE | DQX | 1994-07-20 | View |
| 510(k) | K940814 | HYDRO-M(TM) WOUND GEL | MGQ | 1994-05-12 | View |
| 510(k) | K940738 | KTI HY-Q(TM) WOUND DRESSING | KMF | 1994-05-06 | View |
| 510(k) | K925660 | KTI TRANSPARENT WOUND DRESSING | MGP | 1993-04-20 | View |
| 510(k) | K921502 | HYSORB WOUND DRESSING | KMF | 1992-09-29 | View |
| 510(k) | K882157 | PANAMEX(TM) URETERAL STENT | FAD | 1988-08-02 | View |
No matching devices.
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