FHC, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories3
Latest Approval2023-09-08
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K231141 | STarFix Designer Software C0265 | QRI | 2023-09-08 | View |
| 510(k) | K200169 | VFS1 Bipolar Electrosurgical Generator | GEI | 2020-05-14 | View |
| 510(k) | K183123 | microTargeting Guideline 4000 5.0 System | GZL | 2018-12-20 | View |
No matching devices.