Aperio Technologies Inc

FDA Regulatory Profile

Aperio Technologies Inc appears in FDA public data with 1 recall, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1549-2013, Class II) was initiated on February 22, 2013. Its most recent 510(k) clearance was granted on August 14, 2009.

Summary

Total Recalls
1
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1549-2013Class IIAperio ScanScope System. Aperio ScanScope Models, XT, AT, AT Turbo, CS and CSO. Automated digital sFebruary 22, 2013

Recent 510(k) Clearances

K-NumberDeviceDate
K080564SCANSCOPE XT SYSTEMAugust 14, 2009
K080254SCANSCOPE XT SYSTEMOctober 31, 2008
K073677SCANSCOPE XT SYSTEMAugust 1, 2008
K071671SCANSCOPE XT SYSTEMDecember 28, 2007
K071128SCANSCOPE XT SYSTEMOctober 10, 2007