# Aperio Technologies

- Location (FDA's records): Vista, CA
- FDA decisions: 5 (2007–2009): 5 510(k) clearances
- Product codes: NOT (2), OEO (2), NQN (1)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 8 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Chroma Vision Medical Systems, Inc.: 3 (https://510kreport.com/company/chroma-vision-medical-systems)
- Applied Imaging Corp.: 2 (https://510kreport.com/company/applied-imaging)

## Firms that cite its devices most
- Ventana Medical Systems, Inc.: 2 (https://510kreport.com/company/ventana-medical-systems)
- Leica Biosystems Imaging, Inc.: 2 (https://510kreport.com/company/leica-biosystems-imaging)
- Omnyx, LLC: 1 (https://510kreport.com/company/omnyx)
- Olympus America Inc. / Scientific Equipment Group: 1 (https://510kreport.com/company/olympus-america-scientific-equipment-group)
- Philips Medical Systems Nederland B.V.: 1 (https://510kreport.com/company/philips-medical-systems-nederland)

## Its most-cited devices
- K071671: Scanscope XT System (2007), cited by 4
- K073677: Scanscope XT System (2008), cited by 2
- K080564: Scanscope XT System (2009), cited by 1
- K071128: Scanscope XT System (2007), cited by 1

## Recent decisions
- K080564: Scanscope XT System (Aug 14, 2009)
- K080254: Scanscope XT System (Oct 31, 2008)
- K073677: Scanscope XT System (Aug 1, 2008)
- K071671: Scanscope XT System (Dec 28, 2007)
- K071128: Scanscope XT System (Oct 10, 2007)

Source page: https://510kreport.com/company/aperio-technologies