Enterix, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Advertisement
Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K170548 | InSure ONE | KHE | 2017-10-05 | View |
| 510(k) | K060930 | INSURE II | KHE | 2006-05-04 | View |
| 510(k) | K002457 | !NSURE FECAL OCCULT BLOOD TEST | KHE | 2001-01-12 | View |
No matching devices.
Advertisement