Biovision AG
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K042083 | MODIFICATION TO VISITOME 20-10 MICROKERATOME | HNO | 2004-11-16 | View |
| 510(k) | K014000 | VISTITOME 20-10 MICROKERATOME | HNO | 2002-03-11 | View |
No matching devices.
Advertisement