Company ยท US
Aperio Technologies
FDA 510(k) clearances and medical device recalls filed under this name, 2007 to 2009. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 14, 2009 | K080564 | SCANSCOPE XT SYSTEM Aperio Technologies | NOT |
| Oct 31, 2008 | K080254 | SCANSCOPE XT SYSTEM Aperio Technologies | OEO |
| Aug 1, 2008 | K073677 | SCANSCOPE XT SYSTEM Aperio Technologies | NQN |
| Dec 28, 2007 | K071671 | SCANSCOPE XT SYSTEM Aperio Technologies | OEO |
| Oct 10, 2007 | K071128 | SCANSCOPE XT SYSTEM Aperio Technologies | NOT |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 17, 2013 | Aperio Technologies Inc Aperio ScanScope System. Aperio ScanScope Models, XT, AT, AT Turbo, CS and CSO.
Automated digital slide creation and viewing device.
It is intended to create and view electronic image files represen Terminated |
IBM | None listed |