Scion Medical Technologies, LLC
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2017-04-27
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K170905 | Star Tissue Marker | NEU | 2017-04-27 | View |
| 510(k) | K161234 | CASSI II Rotational Core Biopsy System | KNW | 2016-08-03 | View |
No matching devices.