# Activiews, Ltd.

- Location (FDA's records): Washington, DC
- FDA decisions: 3 (2011–2012): 3 510(k) clearances
- Product codes: JAK (3)
- Predicates its devices cite: 5 (3 its own); citations of its devices by later devices: 3 (3 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
- Veran Medical Technologies, Inc.: 1 (https://510kreport.com/company/veran-medical-technologies)
- Ultraguide, Ltd.: 1 (https://510kreport.com/company/ultraguide)

## Its most-cited devices
- K110812: CT-Guide Needle Guidance System (2011), cited by 2
- K113063: CT-Guide Needle Guidance System (2011), cited by 1

## Recent decisions
- K120300: CT-Guide Needle Guidance System (Apr 13, 2012)
- K113063: CT-Guide Needle Guidance System (Nov 10, 2011)
- K110812: CT-Guide Needle Guidance System (Jun 21, 2011)

Source page: https://510kreport.com/company/activiews