Upstream Peripheral Technologies, Ltd.
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) | K211802 | GoBack Crossing Catheter | PDU | 2022-03-01 | View |
| 510(k) | K182937 | Upstream GoBack Crossing Catheter | DQY | 2019-05-23 | View |
No matching devices.
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