S&G Biotech, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest Approval2025-06-25
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K242845 | EGIS Biliary Double Bare Stent (BDB080405) | FGE | 2025-06-25 | View |
| 510(k) | K223354 | EGIS Biliary Single Bare Stent | FGE | 2023-09-21 | View |
No matching devices.