Boston Scientific Corporation Northwest Technology
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) | K003398 | WIRECLIP TORQUER | DQX | 2000-12-01 | View |
| 510(k) | K993648 | ROTABLATOR ROTATIONAL ANGIOPLASTY SYSTEM WITH THE ROTALINK EXCHANGEABLE CATHETER | MCW | 1999-11-24 | View |
No matching devices.
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