Medical Device Manufacturer · US , Vista , CA

Aperio Technologies - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2007
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Aperio Technologies Pathology ✕
5 devices
1-5 of 5
Cleared Aug 14, 2009
SCANSCOPE XT SYSTEM
K080564 · NOT
Pathology · 533d
Cleared Oct 31, 2008
SCANSCOPE XT SYSTEM
K080254 · OEO
Pathology · 274d
Cleared Aug 01, 2008
SCANSCOPE XT SYSTEM
K073677 · NQN
Pathology · 217d
Cleared Dec 28, 2007
SCANSCOPE XT SYSTEM
K071671 · OEO
Pathology · 192d
Cleared Oct 10, 2007
SCANSCOPE XT SYSTEM
K071128 · NOT
Pathology · 170d
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