Corbin Clinical Resources, LLC
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest Approval2016-09-02
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K160423 | Perineologic Access Needle | FCG | 2016-09-02 | View |
| 510(k) | K160414 | Precision Point Biopsy Needle Guide | ITX | 2016-08-01 | View |
No matching devices.