Accutech Medical Technologies, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K090281 | ACCUTECH FAMILY OF POWERFLEX LASER DELIVERY DEVICES | GEX | 2009-03-04 | View |
| 510(k) | K061025 | ACCUTECH ENDOLITE PROBE | FFS | 2006-05-31 | View |
No matching devices.
Advertisement